Comparison of Two Different Approaches in the Surgical Treatment of Tubal Ectopic Pregnancy

Learn more about:
Related Clinical Trial
Medical Treatment in Ectopic Tubal Pregnancy Evaluation of Different Doses of Letrozole in Ectopic Pregnancy Evaluation of Ipsilateral Tubal Patency After Conservative Medical or Surgical Treatment. Improving Mental Health Following Early PREgnancy Loss Using a Brief Cognitive Task Expectant Management of Ectopic Pregnancy Psychological Impact of Pregnancy of Unknown Location Assessment of Biomarkers in Pregnancy on Unknown Location and Ectopic Pregnancy Comparative Study on the Efficacy of Ovarian Stimulation Protocols on the Success Rate of ICSI in Female Infertility Hysteroscopic Metroplasty in Unexplained Infertile Women With Dysmorphic Uterus Cornual Wedge Resection Outcome Pregnancies of Uncertain Location or Viability Research Randomized Population-Based Study on Chlamydia Trachomatis Screening Sonographic Assessment and Visualization of Ectopics in Emergency Medicine Kisspeptin Levels in Early Pregnancy RCT for Women With a Persisting Pregnancy of Unknown Location Optimal Treatment for Women With a Persisting Pregnancy of Unknown Location Activin A and Inhibin A in Predicting Outcome of Pregnancies of Unknown Location After Assisted Reproductive Technology Evaluation of the Axonemal Dynein Heavy Chain 5 and Creatine Kinase Concentration in Cervical Fluid for Early Detection of the Ectopic Pregnancy Vitamin D in Ectopic Pregnancies Laparoscopic Tubal Preservation Surgery BHCG Level in Day 4,7, in Comparison to Day 10 as an Indicator for Treatment Success The Correlation Between Uterine Endometrial Pattern and Ectopic Pregnancy Adnexal Mass After Methotrexate Treatment for Ectopic Pregnancies The Impact of Salpingectomy and Single Dose Systemic Methotrexate Treatments on Ovarian Reserve in Ectopic Pregnancy Effectiveness Of Expectant Management In The Tubal Ectopic Pregnancy Methotrexate Treatment for Ectopic Pregnancy Comparison of Two Different Approaches in the Surgical Treatment of Tubal Ectopic Pregnancy Two-Dose Methotrexate for Ectopic Pregnancy Ectopic Pregnancy Biomarkers The Aromatase Inhibitor and Gnrh Antagonist Versus Methotrexate for Management of Undisturbed Ectopic Pregnancy Are Serum Levels of Vascular Endothelial Growth Factor a Marker for the Early Diagnosis of Ectopic Pregnancy? Risk Factors of Ectopic Pregnancy Assessment of Biomarkers in Ectopic Pregnancy Risk of Ectopic Pregnancy and Variation of Luteal Estradiol and Progesterone Levels in IVF

Brief Title

Comparison of Two Different Approaches in the Surgical Treatment of Tubal Ectopic Pregnancy

Official Title

Comparison of Conventional Laparoscopy and Natural Orifice Transluminal Endoscopic Surgery in the Surgical Treatment of Tubal Ectopic Pregnancy

Brief Summary

      In this study we aim to compare conventional laparoscopy and natural orifice transluminal
      endoscopic surgery in the surgical treatment of ectopic pregnancy.

      All the patients, with an indication of surgery for ectopic pregnancy, will be asked to
      participate in this clinical trial.

      Indication of surgery will be based on clinical findings, ultrasound scans and serum hcg
      levels. There will be no exclusion criteria.

      Duration of surgery, successful completion of the operation, intraoperative data and
      postoperative data will be collected.

      All the patients will be asked to fill out quality of recovery-40 (QoR-40) questionnaire and
      36-item short form health survey (SF-36) before surgery.

      QoR-40 questionnaire will be repeated 24 hours after surgery and repeated every 24 hours
      until discharge. SF-36 will be repeated at 1-month follow-up visit. Patients will be also
      evaluated at postoperative 3-months, and female sexual function index will be asked to be
      filled-out.
    



Study Type

Interventional


Primary Outcome

Successful completion of surgery as intended

Secondary Outcome

 Quality of Recovery-40 questionnaire

Condition

Ectopic Pregnancy

Intervention

Salpingectomy

Study Arms / Comparison Groups

 Conventional laparoscopy
Description:  In this arm, patients will be treated via conventional laparoscopy

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information


Recruitment Status

Procedure

Estimated Enrollment

40

Start Date

February 19, 2020

Completion Date

May 19, 2021

Primary Completion Date

February 19, 2021

Eligibility Criteria

        Inclusion Criteria:

          -  Adults over 18 years of age,

          -  Diagnosis of tubal ectopic pregnancy

          -  Patient's preference to undergo salpingectomy

        Exclusion Criteria:

          -  Patients with contraindication to endoscopic surgery

          -  Refusal to sign informed consent.
      

Gender

Female

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

, +905330922020, [email protected]

Location Countries

Turkey

Location Countries

Turkey

Administrative Informations


NCT ID

NCT04315779

Organization ID

20-2.1T/40


Responsible Party

Principal Investigator

Study Sponsor

Ege University


Study Sponsor

, , 


Verification Date

March 2020