ClinicalTrials.gov
 Home    Search    Study Topics    Glossary  
 

  Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Incretin Secretion in Women With Polycystic Ovary Syndrome (PCOS)

This study has been terminated.

Sponsors and Collaborators: Hvidovre University Hospital
University of Copenhagen
Information provided by: Hvidovre University Hospital
ClinicalTrials.gov Identifier: NCT00647023
  Purpose

The incretin hormones are secreted from the gastrointestinal tract in response to nutrient ingestion, and are responsible for 70 % of insulin secretion in response to glucose. The incretin response is attenuated in subjects with type 2 diabetes and other conditions associated with insulin resistance. Polycystic ovary syndrome (PCOS) is characterised by irregular periods and increased androgen levels. It is the most common endocrine disorder amongst young women at fertile age, and the most common cause of female infertility. Insulin resistance plays an important role in the development of the disease, and women with PCOS are at increased risk of developing tyoe 2 diabetes. the incretin hormones have not previously been investigated in women with PCOS, and the purpose of the present study was to investigate the secretion of the two most important incretin hormones Glucose-like peptide-1 (GLP-1) and Glucose dependent insulinotropic peptide (GIP) during a three hour oral glucose tolerance test.


Condition Intervention
Polycystic Ovary Syndrome
Drug: metformin

MedlinePlus related topics:   Diabetes   

ChemIDplus related topics:   Metformin    Metformin hydrochloride   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Basic Science

Further study details as provided by Hvidovre University Hospital:

Enrollment:   66
Study Start Date:   February 2004
Study Completion Date:   May 2006
Primary Completion Date:   May 2006 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
A: Experimental Drug: metformin
1000 mg metformin x 2 daily during 8 months

  Eligibility
Ages Eligible for Study:   18 Years to 38 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  • Subjects who fulfill the Rotterdam criteria for PCOS. Age 18-38

Exclusion Criteria:

  • Other endocrine diseases or diseases known to influence glucose/insulin/fat metabolism
  • Oral contraceptive administration within three months of study start
  Contacts and Locations

No Contacts or Locations Provided
  More Information


Responsible Party:   Pernille Fog Svendsen ( Incretin secretion in women with PCOS )
Study ID Numbers:   Incretins and PCOS
First Received:   March 26, 2008
Last Updated:   March 26, 2008
ClinicalTrials.gov Identifier:   NCT00647023
Health Authority:   Denmark: The Regional Committee on Biomedical Research Ethics

Study placed in the following topic categories:
Genital Diseases, Female
Gonadal Disorders
Metformin
Polycystic Ovary Syndrome
Endocrine System Diseases
Endocrinopathy
Ovarian Diseases
Cysts
Ovarian Cysts

Additional relevant MeSH terms:
Neoplasms
Hypoglycemic Agents
Pathologic Processes
Disease
Syndrome
Physiological Effects of Drugs
Pharmacologic Actions
Adnexal Diseases

ClinicalTrials.gov processed this record on October 14, 2008




Links to all studies - primarily for crawlers