Programme of Acromegaly Screening in Patients With Associated Somatic Disorders

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Acromegaly
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Novartis Pharmaceuticals – Acromegaly
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Treatment Patterns and Treatment Outcomes for Acromegaly Ectopic Lipid Deposition and Insulin Resistance in After Treatment of Acromegaly Physiopathology of Sodium Retention in Acromegaly Somatuline® Depot (Lanreotide) for Acromegaly Post-Marketing Observational Study Peri- and Post-operative Dynamics of the Growth Hormone Axis in Subjects With Acromegaly During the First Year After Surgical Resection The Longitudinal Approach to Acromegaly: A Pattern of Treatment and Comparative Effectiveness Research Preoperative Octreotide Treatment of Acromegaly The Treatment and Natural History of Acromegaly Bone MicroArchitecture in Acromegaly Reproducibility and Utility of OGTT in Acromegaly A Prospective Study of Outcome After Therapy for Acromegaly Epidemiology of Acromegaly in Denmark 1991-2010 Programme of Acromegaly Screening in Patients With Associated Somatic Disorders Acromegaly: Patient And Physician Perspectives

Brief Title

Programme of Acromegaly Screening in Patients With Associated Somatic Disorders

Official Title

Programme of Acromegaly Screening in Patients With Associated Somatic Disorders, Who Are Observed at the Moscow Board of Health Endocrinology Dispensary and Endocrinology Hospital at First Moscow State Medical University for the Purpose of Early Identification of the Disease.

Brief Summary

      The primary objective of the protocol is to define percentage of patients with acromegaly in
      relation to the total number of screened patients with confirmed clinically significant set
      of associated somatic disorders with the help of laboratory (Insulin-like Growth Factor I,
      Growth Hormone, Oral Glucose-Tolerance Test [IGF-1, GH, OGTT]) and instrumental examination
      methods (Magnetic Resonance Imaging [MRI]).

Study Type

Observational

Primary Outcome

Percentage of Participants Diagnosed With Acromegaly

Secondary Outcome

 Number of Participants Diagnosed With Acromegaly Using Biochemical Assays (IGF-1, GH, OGTT) and Instrumental Examination Methods (MRI)

Condition

Acromegaly

Intervention

Non-interventional cross-sectional survey

Study Arms / Comparison Groups

 Acromegaly patients
Description:

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

Other

Estimated Enrollment

367

Start Date

December 5, 2013

Completion Date

September 15, 2015

Primary Completion Date

September 15, 2015

Eligibility Criteria

        Inclusion Criteria:

          -  Men and women aged 18 years and above with associated somatic disorders observed at
             the Moscow Endocrinology dispensary or Endocrinology Hospital at First Moscow State
             Medical University

          -  Patients who signed the Informed Consent Form for participation in the survey before
             collection of any information.

        Exclusion Criteria:

          -  Patient already diagnosed with acromegaly

          -  Patient's refusal to participate in the survey.

Gender

All

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Ipsen Medical Director, ,

Location Countries

Russian Federation

Location Countries

Russian Federation

Administrative Informations

NCT ID

NCT02020967

Organization ID

A-38-52030-280

Responsible Party

Sponsor

Study Sponsor

Ipsen

Study Sponsor

Ipsen Medical Director, Study Director, Ipsen

Verification Date

May 2021