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Sickle Cell Pro-Inflammatory Response to Interval Training Study Comparison of Patient Centered Outcomes for People With Sickle Cell Disease in the Acute Care Setting Haploidentical PBMC Transplant for Severe Congenital Anemias Transcranial Doppler (TCD) With Transfusions Changing to Hydroxyurea Neutrophil Extracellular Traps and Sickle Cell Disease A Study of Oral L-citrulline in Sickle Cell Disease LCI-HEM-SCD-ST3P-UP-001: The Sickle Cell Trevor Thompson Transition Project (ST3P-UP Study) Vitamin D for Sickle Cell High-flow Oxygen for Vaso-occlusive Pain Crisis Intermittent Preventive Treatment for Malaria in Patient With Sickle Cell Disease Rifaximin to Modify the Disease Course in Sickle Cell Disease New Hemolysis Parameters in Sickle Cell Disease Phase III Randomized Study of Poloxamer 188 for Vaso-Occlusive Crisis of Sickle Cell Disease Study of Clotrimazole and Hydroxyurea in Patients With Sickle Cell Syndromes Blood Flow and Pain Crises in People With Sickle Cell Disease Assessment of Opioid Analgesia in Sickle Cell Topical Sodium Nitrite in Sickle Cell Disease and Leg Ulcers Sparing Conversion to Abnormal TCD (Transcranial Doppler) Elevation (SCATE) Sickle Cell Clinical Research and Intervention Program Long Term Effects of Erythrocyte Lysis Parent Willingness to Participate in Tobacco Trials in the Pediatric Clinical Setting A Study Evaluating the Safety and Efficacy of the LentiGlobin BB305 Drug Product in Severe Sickle Cell Disease Apixaban in Patients With Sickle Cell Disease Non-Myeloablative Conditioning and Bone Marrow Transplantation An Extension Study to Further Evaluate the Safety, Tolerability of GBT440 in Patients With Sickle Cell Disease Who Participated in the Study GBT440-001 Parent Educational Program for Children With Sickle Cell Disease Acute Kidney Injury in Patients With Sickle Cell Disease Music Therapy in Sickle Cell Pain Mixed Methods Study Improving Parental Psychosocial Functioning and Early Developmental Outcomes in Children With Sickle Cell Disease Phase I/II Randomized Study of Hydroxyurea With or Without Clotrimazole in Patients With Sickle Cell Anemia Shared-Decision Making for Hydroxyurea Inhaled Mometasone to Reduce Painful Episodes in Patients With Sickle Cell Disease BEATS 2: Music Therapy in Sickle Cell Abatacept for GVHD Prophylaxis After Hematopoietic Stem Cell Transplantation for Pediatric Sickle Cell Disease Nonmyeloablative Stem Cell Transplant in Children With Sickle Cell Disease and a Major ABO-Incompatible Matched Sibling Donor A Safety and Efficacy Study Evaluating CTX001 in Subjects With Severe Sickle Cell Disease Sleep Study in Adult Patients With Major Sickle Cell Disease With Paroxysmal Nocturnal Events Curative Versus Disease-Modifying Therapies in Children With Severe Sickle Cell Disease To Assess Safety, Tolerability and Physiological Effects on Structure and Function of AXA4010 in Subjects With Sickle Cell Disease Expanded Access to Voxelotor for Patients With Sickle Cell Disease Who Have No Alternative Treatment Options Safety Of Rivipansel (GMI-1070) In The Treatment Of One or More Vaso-occlusive Crises In Hospitalized Subjects With Sickle Cell Disease Nonmyeloablative Peripheral Blood Mobilized Hematopoietic Precursor Cell Transplantation for Sickle Cell Disease and Beta-thalassemia in People With Higher Risk of Transplant Failure Effects of HQK-1001 in Patients With Sickle Cell Disease Patient-Provider Tools to Improve the Transition to Adult Care in Sickle Cell Disease A Study of HQK-1001 in Patients With Sickle Cell Disease Study of Propranolol as Anti-Adhesive Therapy in Sickle Cell Disease (SCD) Hemoglobin Desaturation in Sickle Cell Disease Evaluation of Spectra Optia Red Blood Cell Exchange in Sickle Cell Patients Pediatric Open-Label Extension of Voxelotor Pulmonary Hypertension in Patients With Sickle Cell Disease in Nigeria Integration of mHEALTH Into the Care of Patients With Sickle Cell Disease to Increase Hydroxyurea Utilization Iron Overload Assesment in Sickle Cell Anemia and Sickle Cell Thalassemia Steroid Treatment for Sickle Cell Pain Crisis Epidemiology and Pathophysiological Mechanisms of HTAP in SS and SC Children in Martinique and Guadeloupe. Heart Arteries and Sickle Cell Disease / Coeur Artères DREpanocytose Epidemiology of Silent and Overt Strokes in Sickle Cell Disease Microvascular and Cardiac Dysfunction in Paroxysmal Nocturnal Hemoglobinuria and Sickle Cell Disease Assessing the Safety of Buprenorphine in People With Sickle Cell Disease A Blood Stem Cell Transplant for Sickle Cell Disease Central Nervous System Vascular Changes in Adult Sickle Cell Disease and the Effect of Treatment With Simvastatin Efficacy and Safety of Ferriprox® in Patients With Sickle Cell Disease or Other Anemias Evaluation of Knowledge Among Adolescents With Sickle Cell Disease. Dose Escalation Study to Evaluate the Safety, Tolerability, PK and PD of Voxelotor in Patients With SCD Computerized Cognitive Behavioral Therapy Assisted Life Management for Pain in Sickle Cell Disease Single-center Prospective Evaluation of Sickle Cell Patient Care in the CHU Brugmann Emergency Department Long-term Safety and Efficacy of Ferriprox® in Iron Overloaded Patients With Sickle Cell Disease or Other Anemias Intranasal Ketamine For Pain Control In Patients With Sickle Cell Disease And Vaso-occlusive Episode (VOE) In The PED Tricuspid Regurgitant Jet Velocity as an Independent Marker for Mortality in Sickle Cell Anemia Management of Severe Acute Malnutrition in SCD, in Northern Nigeria Improving Sickle Cell Disease (SCD) Care Using Web-based Guidelines A Study of Patients Having Pulmonary Hypertension Associated With Sickle Cell Disease and Completing an ASSET Study Implication of the Oxydative Stress in the Pathophysiology of Sickle Cell Anemia: SCD-Haplo: Phase II Study of HLA-Haploidentical SCT for Aggressive SCD A Study of the Safety, Blood Levels and Biological Effects of GBT440 in Healthy Subjects and Subjects With Sickle Cell Disease Study of Methodologies to Measure Blood Flow and Oxygenation in Adults With Sickle Cell Disease Nitric Oxide Therapy for Acute Chest Syndrome in Sickle Cell Disease Children T-Cell Depleted Alternative Donor Bone Marrow Transplant for Sickle Cell Disease (SCD) and Other Anemias Hydroxyurea and Erythropoietin to Treat Sickle Cell Anemia Functional Neuroimaging of Pain Using EEG and fMRI Study of Deferasirox Relative to Subcutaneous Deferoxamine in Sickle Cell Disease Patients Arginine Therapy for Sickle Cell Disease Pain A SAD/MAD to Assess the Safety, Pharmacokinetics and Pharmacodynamics of FT-4202 in Healthy Volunteers and Sickle Cell Disease Patients Effect of Virtual Reality Technology for Pain Management of Vaso-Occlusive Crisis in Patients With Sickle Cell Disease Effectiveness of a Computerized Tool (PAINRelieveIt) to Help Manage Pain Related to Sickle Cell Disease A Stratified Sickle Event Randomized Trial (ASSERT) Decompression Coring Versus Conservative Therapy in Patients With Avascular Necrosis of the Hip Related to Sickle Cell Disease An Extension Study of IMR-687 in Adult Patients With Sickle Cell Anemia Screening Patients With Sickle Cell Disease for Kidney Damage Defibrotide in Sickle Cell Disease-Related Acute Chest Syndrome Androgen Regulation of Priapism in Sickle Cell Disease A Study of the Effect of IW-1701 (Olinciguat), a Stimulator of Soluble Guanylate Cyclase (sGC), on Patients With Sickle Cell Disease (SCD) Adherence to Hydroxyurea in Children With Sickle Cell Anemia iCanCope With Sickle Cell Pain Sickle Cell Anemia and Cerebral Microcirculation : Multimodal Exploration Autologous Bone Marrow Stem Cell Transplantation for Osteonecrosis in Sickle Cell Disease ElectroNic Hydroxyurea AdhereNCE: A Strategy to Improve Hydroxyurea Adherence in Patients With Sickle Cell Disease Comparison of Allogeneic Matched Related Haematopoietic Stem Cell Transplantation After a Reduced Intensity Conditioning Regimen With Standard of Care in Adolescents and Adults With Severe Sickle Cell Disease Mesenchymal Stromal Cells for Haplo Hematopoietic Cell Transplantation for Sickle Cell Disease Study of HLA-Haploidentical Stem Cell Transplantation to Treat Clinically Aggressive Sickle Cell Disease Using Patient-Centered Guidelines in a Technology Platform to Improve Health Care in Adults With Sickle Cell Disease Evaluation of a Training Program for Homozygous Sickle Cell Disease Patients Effect of Exercise With and Without HMB on Body Composition and Muscle Strength in Sickle Cell Anaemia Safety and Efficacy of Gene Therapy of the Sickle Cell Disease by Transplantation of an Autologous CD34+ Enriched Cell Fraction That Contains CD34+ Cells Transduced ex Vivo With the GLOBE1 Lentiviral Vector Expressing the βAS3 Globin Gene in Patients With Sickle Cell Disease (DREPAGLOBE) Impact on the Length of Stay in Incentive Spirometry and Pain in the Decompensation of Sickle Cell Disease: . Transfusion in Sickle Cell Disease: Screening of Sickle Cell Disease Trait in Blood Donors Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Escalating Multiple Oral Doses of AG-348 in Subjects With Stable Sickle Cell Disease A Single Dose Study of the Safety, Blood Levels and Biological Effects of Aes-103 Compared to Placebo in Subjects With Stable Sickle Cell Disease The Brigance Assessment Of Individual Neurodevelopment In Young Children With Sickle Cell Disease- 2 Comparing Individualized vs. Weight Based Protocols to Treat VOE in SCD Occlusive Episodes in Sickle Cell Disease Cognitive Rehabilitation in Sickle Cell Disease The Effect of Rivaroxaban in Sickle Cell Disease Muscle Function and Its Biological and Physiological Determinants in Sickle Cell Disease Safety of Single Ascending Doses of CSL889 in Adult Patients With Stable Sickle Cell Disease Sickle Cell Disease and CardiovAscular Risk – Red Cell Exchange Trial (SCD-CARRE) Dose-Finding Study of SC411 in Children With Sickle Cell Disease A Pilot Study on Neuroimaging in SCD: Part of The Boston Consortium to Cure Sickle Cell Disease Low-Dose Ketamine Infusion for Children With Sickle Cell Disease-Related Pain Pathophysiology of Acute Pain in Patients With Sickle Cell Disease Implications of a Paediatrician-psychologist Tandem for Sickle Cell Disease Care and Impact on Cognitive Functioning Vascular Function Intervention Trial in Sickle Cell Disease A Study Evaluating Gene Therapy With BB305 Lentiviral Vector in Sickle Cell Disease Decitabine for High-Risk Sickle Cell Disease Acceptability, Feasibility and Safety of a Yoga Program for Chronic Pain in Sickle Cell Disease Vaporized Cannabis for Chronic Pain Associated With Sickle Cell Disease Effectiveness of Laying-on-of-hands for Sickle Cell Disease Improving Self-Management in Adolescents With Sickle Cell Disease Sulfadoxine- Pyrimethamine Versus Weekly Chloroquine for Malaria Prevention in Children With Sickle Cell Anemia Decision Aid for Therapeutic Options In Sickle Cell Disease Phase 1/2 Study to Evaluate the Safety, Tolerability and Pharmacokinetics of HQK-1001 Administered Daily in Patients With Sickle Cell Disease Glucose Metabolism in Sickle Cell Disease Sildenafil Therapy for Pulmonary Hypertension and Sickle Cell Disease Improving Disease Knowledge in Adolescents With Sickle Cell Disease Sickle Cell Anemia – A Comparative Study Between Three Ethnical Communities, a Multicenter Study Effect of Atorvastatin on Endothelial Dysfunction and Albuminuria in Sickle Cell Disease Haploidentical Hematopoietic Stem Cell Transplantation (HSCT) for Patients With Severe Sickle Cell Disease Adenosine 2A Agonist Lexiscan in Children and Adults With Sickle Cell Disease Trial of Zileuton CR in Children and Adults With Sickle Cell Disease Efficacy of Vorinostat to Induce Fetal Hemoglobin in Sickle Cell Disease Transfusion in Sickle Cell Disease: Risk Factors for Alloimmunization Patient Centered Comprehensive Medication Adherence Management System in Patients With Sickle Cell Disease Gene Transfer for Sickle Cell Disease Risk-based Therapy for Sickle Cell Anemia: A Feasibility Study Study to Evaluate the Effect of Voxelotor Administered Orally to Patients With Sickle Cell Disease (GBT_HOPE) Feasibility of a Stress Reduction Intervention Study in Sickle Cell Disease Ketamine as an Adjuvant Therapy for Acute Vaso Occlusive Crisis in Pediatric Patients With Sickle Cell Disease Collect of Cord Blood From Subjects at Risk for Sickle Cell Disease, for the Purpose of Laboratory Research Escalation of Plerixafor for Mobilization of CD34+ Hematopoietic Progenitor Cells and Evaluation of Globin Gene Transfer in Patients With Sickle Cell Disease Pilot Study on the Effects of Intravenous Ketamine on Acute Pain Crisis in Patients With Sickle Cell Disease Effects of Nitric Oxide and Nitroglycerin in Patients With Sickle Cell Anemia Nonmyeloablative Conditioning for Mismatched Hematopoietic Stem Cell Transplantation for Severe Sickle Cell Disease Heart Disease in Sickle Cell Anemia Study of Decitabine and Tetrahydrouridine (THU) in Patients With Sickle Cell Disease A Reduced Toxicity Allogeneic Unrelated Donor Stem Cell Transplantation (SCT) for Severe Sickle Cell Disease Study Exploring the Effect of Crizanlizumab on Kidney Function in Patients With Chronic Kidney Disease Caused by Sickle Cell Disease A Pilot Study of Fecal Microbiome and Neutrophil Cellular Adhesion Molecules in Patients With Sickle Cell Disease (SCD) A Study of Nicotinamide With Oral Tetrahydrouridine and Decitabine to Treat High Risk Sickle Cell Disease A Study of SHP655 (rADAMTS13) in Sickle Cell Disease A Phase Ib Study of NVX-508 in Sickle Cell Disease SACRED A Prospective Research Study to Reduce Stroke in Children With Sickle Cell Anemia A Study to Assess the Safety, Tolerability, and Efficacy of BIVV003 for Autologous Hematopoietic Stem Cell Transplantation in Patients With Severe Sickle Cell Disease TRF-1101 Assessment in Sickle Cell Disease Study of Dose Confirmation and Safety of Crizanlizumab in Pediatric Sickle Cell Disease Patients The Spleen in Sickle Cell Anemia and Sickle Cell Thalassemia Repeat Peripheral Blood Stem Cell Transplantation for Patients With Sickle Cell Disease and Falling Donor Myeloid Chimerism Levels Immunogenicity Study of an Anti-pneumococcal Vaccination Strategy in Patients With Sickle Cells Disease The Implementation of the Automated Erythrocytapheresis in Egyptian Sickle Cell Disease Center Acupuncture for Pain in Sickle Cell Disease Nonmyeloablative Haploidentical Peripheral Blood Mobilized Hematopoietic Precursor Cell Transplantation for Sickle Cell Disease Macitentan in Pulmonary Hypertension of Sickle Cell Disease Exhaled Carbon Monoxide as a Marker of Hemolysis in Sickle Cell Disease- an Exploratory Study Hydroxyurea to Prevent Brain Injury in Sickle Cell Disease Gum Arabic as Fetal Hemoglobin Agent in Sickle Cell Anemia Pharmacokinetics (PK) of Liquid Hydroxyurea in Pediatric Patients With Sickle Cell Anemia Pain Management in Children and Young Adults With Sickle Cell Disease Clinical Trial to Study the Safety and Tolerability of Memantin Mepha® in Sickle Cell Disease Patients Assessing Function in Pediatric Patients With Sickle Cell Disease Hepcidin Levels in Sickle Cell Disease (SCD) A Study of IMR-687 in Adult Patients With Sickle Cell Anaemia (Homozygous HbSS or Sickle-β0 Thalassemia) European Sickle Cell Disease Cohort – Hydroxyurea Predictors and Outcomes in Patients With Sickle Cell Disease Study to Assess Safety and Impact of SelG1 With or Without Hydroxyurea Therapy in Sickle Cell Disease Patients With Pain Crises SMYLS: A Self-management Program for Youth Living With Sickle Cell Disease L-Glutamine Therapy for Sickle Cell Anemia Dronabinol for Pain and Inflammation in Adults Living With Sickle Cell Disease Nitric Oxide and Transfusion Therapy for Sickle Cell Patients With Pulmonary Hypertension L-Glutamine Therapy for Sickle Cell Anemia and Sickle ß0 Thalassemia Zinc for Infection Prevention in Sickle Cell Anemia (ZIPS) Web-MAP Intervention for Youth With Sickle Cell Disease Study to Evaluate the Effect of GBT440 in Pediatrics With Sickle Cell Disease Effect of MitoQ on Platelet Function and Reactive Oxygen Species Generation in Patients With Sickle Cell Anemia iPeer2Peer Program for Youth With Sickle Cell Disease Imatinib for Pain in Sickle Cell Anemia Sildenafil for Treatment of Priapism in Men With Sickle Cell Anemia Effect of Ticagrelor vs. Placebo in the Reduction of Vaso-occlusive Crises in Pediatric Patients With Sickle Cell Disease Study of Two Doses of Crizanlizumab Versus Placebo in Adolescent and Adult Sickle Cell Disease Patients Carbon Monoxide Levels and Sickle Cell Disease Severity Myeloablative Conditioning, Prophylactic Defibrotide and Haplo AlloSCT for Patients With Sickle Cell Disease Ibuprofen and Opioid (Morphine or Diamorphine) for Acute Pain in Sickle Cell Disease – Sickle With Ibuprofen & Morphine Peripheral Blood Stem Cell Collection for Sickle Cell Disease (SCD) Patients Treatment of Sickle Cell Anemia With Stem Cell Transplant Neurovascular Determinants of Cognitive Function in Adults With Sickle Cell Disease Stem Cell Transplantation for Sickle Cell Anemia Zinc Supplementation in Children With Sickle Cell Disease in Western Kenya The Feasibility of the PAINReportIt Guided Relaxation Intervention-Outpatient Codeine in Sickle Cell Disease Autologous Bone Marrow Stem Cells for Chronic Leg Ulcer Treatment in Sickle Cell Disease Safety of Blood Stem Cell Mobilization With Plerixafor in Patients With Sickle Cell Disease Tadalafil for Treatment of Priapism in Men With Sickle Cell Anemia N-Acetylcysteine in Patients With Sickle Cell Disease Atorvastatin Therapy to Improve Endothelial Function in Sickle Cell Disease Stem Cell Transplant in Patients With Severe Sickle Cell Disease Study of Blood Platelets in Sickle Cell Disease Clinical and Laboratory Characteristics of Sickle Cell Anemia Patients Admitted With Fever Endothelial Function in Patients With Sickle Cell Anemia Before and After Sildenafil Evaluating Barriers to Stroke Screening and Prevention in Children With Sickle Cell Disease Absorption, Metabolism, and Excretion of a Single Dose of Ferriprox® in Patients With Sickle Cell Disease A Safety Study of Eptifibatide in Patients With Sickle Cell Disease A Study Evaluating the Efficacy and Safety of LentiGlobin BB305 Drug Product in Beta-Thalassemia Major and Sickle Cell Disease Laboratory-based Hypnosis Intervention on Pain Responsivity in Adolescents With Sickle Cell Disease The Link Between Anemia and Deficits in Memory and Attention in Individuals With Sickle Cell Disease The Feasibility of the PAINReportIt Guided Relaxation Intervention-INPATIENT Safety and Efficacy of Sodium Nitrite in Sickle Cell Disease Analysis of T-Cell Immune Reconstitution Following Allogeneic Hematopoietic BMT for Severe SCD Hydroxyurea Adherence for Personal Best in Sickle Cell Disease (HABIT): Efficacy Trial A Study of the Efficacy and Safety of ICA-17043 (With or Without Hydroxyurea) in Patients With Sickle Cell Anemia. Inhaled Corticosteroid Use to Prevent Acute Chest Syndrome Recurrence in Children Between 1 and 4 With Sickle Cell Disease: a Feasibility Trial Cerebrovascular Reserve Measurements in Sickle Cell Disease Examining the Knowledge, Attitudes, and Beliefs of Sickle Cell Disease Patients, Parents of Patients With Sickle Cell Disease, and Providers Towards the Integration of CRISPR in Clinical Care A New Reagent Assay Examining Natural Parvovirus B19 Infection in Sickle Cell Disease MAP to Provide Access to Crizanlizumab, for Sickle Cell Disease Patients A Pilot Study of Azithromycin Prophylaxis for Acute Chest Syndrome in Sickle Cell Disease Efficacy, Safety Study and Benefit of Alkali Therapy in Sickle Cell Disease Nitric Oxide to Improve Blood Flow in Sickle Cell Disease Risk Clinical Stratification of Sickle Cell Disease in Nigeria, Assessment of Efficacy/Safety of Hydroxyurea Treatment The Efficacy of Jobelyn (Sorghum Bicolor Extract)in the Treatment of Sickle Cell Anemia A Rehabilitation Program in Children With Sickle Cell Disease and Cognitive Deficits: a Pilot Study Music Therapy in Sickle Cell Transition Study Evaluation of Hydroxyurea Plus L-arginine or Sildenafil to Treat Sickle Cell Anemia A Study of Prasugrel in Pediatric Participants With Sickle Cell Disease (SCD) Sickle Cell Disease: A Retrospective Chart Review Kidney Function in Sickle Cell Anemia A Multi-Center Study of Riociguat in Patients With Sickle Cell Diseases Sickle Cell Disease Conditioning for Bone Marrow Transplant Study of Beet Juice for Patients With Sickle Cell Anemia Hydroxyurea for the Treatment of Patients With Sickle Cell Anemia Hematopoietic Stem Cell Transplant for Sickle Cell Disease Bone Marrow Transplantation vs Standard of Care in Patients With Severe Sickle Cell Disease (BMT CTN 1503) Kidney Transplantation in Patients With Sickle Cell Disease Simvastatin (Zocor) Therapy in Sickle Cell Disease MUSic Therapy to Improve Quality Of Life in Sickle Cell Disease (MUSIQOLS) Hydroxyurea for Children and Young Adults With Sickle Cell Disease and Pulmonary Hypertension Omega-3 Fatty Acids in Sickle Cell Disease Quantifying the Presence of Lung Disease and Pulmonary Hypertension in Children With Sickle Cell Disease Comparing Acute Pain Management Protocols for Patients With Sickle Cell Disease Vitamin D and Bisphosphonates in the Treatment of Sickle Cell Disease Hypnosis to Manage Pain and Symptoms in Patients With Sickle Cell Disease Exercise-induced Pulmonary Hypertension in Patients With Sickle-cell Anemia HLA Haploidentical Bone Marrow Transplant in Patients With Severe Sickle Cell Disease Bone Marrow Transplantation in Treating Children With Sickle Cell Disease Stem Cell Transplant in Sickle Cell Disease and Thalassemia Evaluation of Different Dose Regimens of Aes-103 Given for 28 Days to Subjects With Stable Sickle Cell Disease Pain Management Protocol for Pediatric Sickle Cell Disease Clinical and Laboratory Assessment of Iron Overload in Sickle Cell Anemia and Sickle Cell Thalassemia Haploidentical Transplantation With Pre-Transplant Immunosuppressive Therapy for Patients With Sickle Cell Disease A Study of Varespladib Infusion in Subjects With Sickle Cell Disease. Sickle Cell Disease and Endothelial Progenitor Cells (EPCs) Acupuncture for Adults With Sickle Cell Disease (SCD): A Feasibility Study Study to Evaluate the Effect of Ticagrelor Versus Placebo in Reducing Vaso-Occlusive Crises Rate in Pediatric Patients With Sickle Cell Disease. Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease A Pilot Study of Chronic Red Blood Cell Transfusion in Sickle Cell Disease-Associated Pulmonary Hypertension Vitamin D Supplementation in Children With Sickle Cell Disease L-Arginine and Sickle Cell Disease Sleep Apnea in Sickle Cell Disease Microvessels and Heart Problems in Sickle Cell Disease Dose-Escalation Study of SCD-101 in Sickle Cell Disease Minimizing Toxicity in HLA-identical Related Donor Transplantation for Children With Sickle Cell Disease Oxygen Therapy and Pregnancy in Sickle Cell Disease A Study to Evaluate Safety, Pharmacokinetic, and Biological Activity of INCB059872 in Subjects With Sickle Cell Disease Novel Cardiac Magnetic Resonance Imaging to Define a Unique Restrictive Cardiomyopathy in Sickle Cell Disease DREPAMASSE Study – Evaluation of a Newborn Screening for Sickle Cell Disease by Tandem Mass Spectrometry Study of Hydroxyurea to Treat Sickle Cell Disease Evaluation of the Prevalence of Pulmonary Hypertension in Adult Patients With Sickle Cell Disease A Phase III Safety and Efficacy Study of L-Glutamine to Treat Sickle Cell Disease or Sickle βo-thalassemia A Study of Prasugrel in Pediatric Participants With Sickle Cell Disease A Phase II Trial of Regadenoson in Sickle Cell Anemia Establishment of Functional MRI Imaging Parameters for Use in the Evaluation of Sickle Cell Disease Aspirin Prophylaxis in Sickle Cell Disease Sickle Cell Disease: Targeting Alloantibody Formation Reduction; Risk Factors, and Genetics The Role of Endothelin-1 in Sickle Cell Disease Adolescent, Caregiver, and Young Adult Perspectives of the Transition From Pediatric to Adult Care for Sickle Cell Disease: A Preliminary Evaluation of the Sickle Cell Disease Transition Program Long Term Effects of Hydroxyurea Therapy in Children With Sickle Cell Disease Neuropathic Pain in Jamaicans With Sickle Cell Disease Families Taking Control (FTC): Family-based Problem-solving Intervention for Children With Sickle Cell Disease Measurement of Cerebral Blood Flow Using Transcranial Doppler Ultrasound in Children With Sickle Cell Disease Study of a Red Blood Cell Deformability Parameter in Patients With Sickle Cell Disease Sickle Cell Disease Biofluid Chip Technology (SCD BioChip) Sleep Respiratory Disorders Evaluation in Sickle Cell Disease Children SMART Mobile Application Technology Utilization in the Treatment of Sickle Cell Disease Post Day Hospital Discharge A Randomized Trial of LOVAZA in Pediatric Sickle Cell Disease (SCD) Stem Cell Transplantation With Identical Donors for Patients With Sickle Cell Disease Study to Evaluate the Effect of GBT440 on TCD in Pediatrics With Sickle Cell Disease A Sickle CEll Disease ComplicatioN Trial Hydroxyurea in Young Children With Sickle Cell Anemia Contraception in Women With Sickle Cell Disease Efficacy of a Decision Aid for Hydroxyurea in Sickle Cell Disease Sickle Cell Disease, Hemechip Transplantation Using Reduced Intensity Approach for Patients With Sickle Cell Disease From Mismatched Family Donors of Bone Marrow Medication Adherence in Youth With Sickle Cell Disease (SCD) The Feasibility of Text Messaging to Assess Secondhand Smoke Exposure Among Youngsters With Cancer or Sickle Cell Disease Study of Efficacy, Safety and Tolerability of ACZ885 (Canakinumab) in Pediatric and Young Adult Patients With Sickle Cell Anemia Inflammatory Response to Hydroxyurea Therapy in Sickle Cell Disease Blood Sampling for Research Related to Sickle Cell Disease Pediatric -Adult Care Transition Program of Patients With Sickle Cell Disease Assessment of Algorithm-Based Hydroxyurea Dosing on Fetal Hemoglobin Response, Acute Complications, and Organ Function in People With Sickle Cell Disease Qualitative Survey of Potential Exercise Activity in Adults With Sickle Cell Anemia (SCA) Sickle Cell Anemia in an Arab Bedouin Village in the Northern Israel Non-Myeloablative Bone Marrow Transplant for Patients With Sickle Cell Anemia and Other Blood Disorders Hydroxyurea in the Treatment of Sickle Cell Disease Study of Panobinostat (LBH589) in Patients With Sickle Cell Disease Study of SANGUINATE™ Versus Hydroxyurea in Sickle Cell Disease (SCD) Patients Effect of Simvastatin Treatment on Vaso-occlusive Pain in Sickle Cell Disease Stem Cell Gene Therapy for Sickle Cell Disease Safety, Pharmacokinetic, and Pharmacodynamic Study of NKTT120 in Adult Patients With Stable Sickle Cell Disease (SCD) A Phase 2 Study of the Effects of 6R-BH4 in Subjects With Sickle Cell Disease State Of The Art Functional Imaging In Sickle Cell Disease Study of Intravenous GMI-1070 in Adults With Sickle Cell Disease Survey in a Population of Sickle Cell Disease Patients to Evaluate the Transition Between the Queen Fabiola Children Hospital and the CHU Brugmann Hospital, and the Quality of the Hospital Care Within the CHU Brugmann Hospital. Study of Ventilatory Mechanics in Patients With Sickle Cell Anemia A Study Evaluating the Long-Term Safety of ICA-17043 in Sickle Cell Disease Patients With or Without Hydroxyurea Therapy Ph I/II Study of Allogeneic SCT for Clinically Aggressive Sickle Cell Disease (SCD) Working Memory and School Readiness in Preschool-Aged Children With Sickle Cell Disease MACS Study – Microparticles and Coagulation in Sickle Cell Disease Haplo T-Cell Depleted Transplantation in High-Risk Sickle Cell Disease A Brief Laboratory-Based Hypnosis Session for Pain in Sickle Cell Disease Prasugrel Versus Placebo in Adult Sickle Cell Disease Evaluating the Safety and Effectiveness of Bone Marrow Transplants in Children With Sickle Cell Disease (BMT CTN 0601) PK Study of Ticagrelor in Children Aged Less Than 24 Months, With Sickle Cell Disease (HESTIA4) Enhancing Use of Hydroxyurea In Sickle Cell Disease Using Patient Navigators Therapeutic Application of Intravascular Nitrite for Sickle Cell Disease PK and PD Responses to Oral L-Citrulline in Patients With Sickle Cell Disease Prevalence of Problematic Use of Equimolar Mixture of Oxygen and Nitrous Oxide and Analgesics in the Sickle-cell Disease Macrolide Therapy to Improve Forced Expiratory Volume in 1 Second in Adults With Sickle Cell Disease Study of Vitamin D in Children With Sickle Cell Disease Psychometric Evaluation of the IPPAQ in Pediatric Patients With Sickle Cell Disease Hospitalized With Vasoocclusive Pain Haploidentical Stem Cell Transplant for Patients With Sickle Cell Disease and Prior Stroke or Abnormal Transcranial Ultrasound Sickle Cell Anemia WE CARE Improving Emergency Department Management of Adults With Sickle Cell Disease Transfusion Alternatives Pre-Operatively in Sickle Cell Disease (TAPS) Exploring Adherence Monitoring in Sickle Cell Disease Niacin to Improve Blood Flow in People With Sickle Cell Disease HLA-Identical Sibling Donor Bone Marrow Transplantation for Individuals With Severe Sickle Cell Disease Using a Reduced Intensity Conditioning Regimen Sickle Cell Disease (SCD) Decision Aid Evaluation of Purified Poloxamer 188 in Vaso-Occlusive Crisis of Sickle Cell Disease (EPIC) Propanolol and Red Cell Adhesion Non-asthmatic Children Sickle Cell Disease Plasma DNA and Vascular Remodelling in Patients With Sickle Cell Disease Spectralis HRA+OCT Imaging of the Retina With Autofluorescence in Sickle Cell Disease A Pilot Study of N-acetylcysteine in Patients With Sickle Cell Disease Carbon Monoxide Measurement to Screen for Sickle Cell Disease SALT: Alternative Donor Bone Marrow and Cord Blood Transplantation for High Risk Sickle Cell Disease Safety and Pharmacokinetics of SANGUINATE™ in Sickle Cell Disease (SCD) Patients Cardiovascular Complications of Sickle Cell Disease Bone Marrow Transplantation in Young Adults With Severe Sickle Cell Disease Quantitative MRI for Patients With Sickle Cell Disease Undergoing Hematopoietic Cell Transplant Exercise Capacity in Pediatric Sickle Cell Anemia A 3-year, Prospective, Non-interventional, Multicenter Registry in Sickle Cell Disease (SCD) Patients Links Between Cognitive Functions and Clinical, Biological and Neuroradiological Outcomes in Adults With Sickle Cell Disease. Molecular Phenotyping of Asthma in Sickle Cell Disease Secondary Pulmonary Hypertension in Adults With Sickle Cell Anemia Liver Fibrosis in Sickle Cell Disease Evaluation of the Lung Capillary Blood Volume in Children With Sickle Cell Disease Evaluation of the Hemostatic Potential in Sickle Cell Disease Patients Longitudinal Changes in Exercise Capacity in Children and Young Adults With Sickle Cell Anemia Sickle Cell Disease – Stroke Prevention in Nigeria Trial Biological, Genetic and Environmental Involved in the Complications of Sickle Cell Disease Community Health Workers and mHealth for Sickle Cell Disease Care Evaluation of Nocturnal Enuresis and Barriers to Treatment Among Pediatric Patients With Sickle Cell Disease Sleep and Pain in Sickle Cell Disease A Study to Assess the Effect of Ticagrelor in Reducing the Number of Days With Pain in Patients With Sickle Cell Disease Gene Transfer for Patients With Sickle Cell Disease Vitamin D3 in Patients With Sickle Cell Disease Collection and Storage of Umbilical Cord Stem Cells for Treatment of Sickle Cell Disease Risk Factors for Allo-immunization in Sickle Cell Disease Phase 1 Study of Zoledronic Acid in Sickle Cell Disease Sickle-cell Disease Registry of the GPOH Microvascular Blood Flow in Sickle Cell Anemia Added Value of Speckle Tracking in the Evaluation of Patients With Sickle Cell Disease

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