Programme of Acromegaly Screening in Patients With Associated Somatic Disorders

NCT ID: NCT02020967

Last Updated: 2021-05-26

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

367 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-12-05

Study Completion Date

2015-09-15

Brief Summary

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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 \[MRI\]).

Detailed Description

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Conditions

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Acromegaly

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Acromegaly patients

Non-interventional cross-sectional survey

Intervention Type OTHER

This is a survey which does not involve any intervention into routine clinical practice, including the use of any investigational therapy or special examination methods.

Interventions

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Non-interventional cross-sectional survey

This is a survey which does not involve any intervention into routine clinical practice, including the use of any investigational therapy or special examination methods.

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ipsen

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ipsen Medical Director

Role: STUDY_DIRECTOR

Ipsen

Locations

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Moscow Board of Health Endocrinology Dispensary

Moscow, , Russia

Site Status

Endocrinology Hospital at First Moscow State Medical University

Moscow, , Russia

Site Status

Countries

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Russia

Other Identifiers

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A-38-52030-280

Identifier Type: -

Identifier Source: org_study_id

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