Lifestyle Intervention and Metformin for Women With Polycystic Ovary Syndrome (PCOS) - Full Text View

Sponsor:	Penn State University
Collaborator:	Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Information provided by:	Penn State University
ClinicalTrials.gov Identifier:	NCT00151411

Purpose

The purpose of this study is to determine if the combination therapy of lifestyle intervention and use of Metformin together will improve ovulation induction and hyperandrogenemia in women with polycystic ovary syndrome, by gathering data from adult and adolescent females.

Condition	Intervention	Phase
Polycystic Ovary Syndrome	Drug: Metformin	Phase II

Study Type:	Interventional
Study Design:	Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator), Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title:	The Effect of Combination Therapy With Lifestyle Intervention and Metformin in Females With Polycystic Ovary Syndrome

Resource links provided by NLM:

Drug Information available for: Metformin Metformin hydrochloride

U.S. FDA Resources

Further study details as provided by Penn State University:

Primary Outcome Measures:

The investigators hypothesize that combination therapy will result in a greater improvement in hyperandrogenemia that single agent therapy.

Secondary Outcome Measures:

The investigators hypothesize that combination therapy will result in a greater improvement in ovulatory frequency and insulin sensitivity that single agent therapy.

Enrollment:	150
Study Start Date:	October 2004
Study Completion Date:	March 2008
Primary Completion Date:	March 2008 (Final data collection date for primary outcome measure)

Detailed Description:

PCOS is characterized by excess circulating androgen levels and chronic anovulation. PCOS is also characterized by insulin resistance and hyperinsulinemia. Several recent studies in a variety of non-hospital based populations have provided evidence that the incidence of hyperandrogenic chronic anovulation is in the range of 4-6% of the female population. Improvements in insulin sensitivity in women with PCOS, either through lifestyle changes or through pharmaceutical intervention, have consistently resulted in a marked improvement in the reproductive and metabolic abnormalities in PCOS. The primary objective in the adult female population is to determine that combination therapy will improve ovulatory frequency. Secondary objective is to improve circulating hyperandrogenemia and insulin sensitivity then single agent therapy. The primary objective of the adolescent population is to determine that the combination therapy will improve hyperandrogenemia. Secondary objective is to improve ovulatory frequency and insulin sensitivity than just the use of a single agent therapy.

Eligibility

Ages Eligible for Study:	12 Years to 39 Years
Genders Eligible for Study:	Female
Accepts Healthy Volunteers:	Yes

Criteria

Inclusion Criteria:

Spontaneous intermenstrual periods of greater than or equal to 45 days or a total of 8 or less periods per year
Elevated testosterone levels
General good health
Off of current medications which may confound response to study medications

Exclusion Criteria:

Pregnancy
Lactose Intolerance
Medical Contraindications
Elevated Prolactin, 17 OHP, or FSH blood tests
Diabetes, liver, heart, kidney or uncorrected thyroid disease

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00151411

Locations

United States, Pennsylvania
Penn State Milton S. Hershey Medical Center
Hershey, Pennsylvania, United States, 17033

Sponsors and Collaborators

Penn State University

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Investigators

Principal Investigator:

Richard Legro, M.D.

Milton S. Hershey Medical Center

More Information

Additional Information:

Click here for more information about this study This link exits the ClinicalTrials.gov site

No publications provided

Responsible Party:	The Pennsylvania State University ( Richard S. Legro, M.D. )
Study ID Numbers:	2003-172, HD-02-012
Study First Received:	September 8, 2005
Last Updated:	August 26, 2009
ClinicalTrials.gov Identifier:	NCT00151411 History of Changes
Health Authority:	United States: Food and Drug Administration

Keywords provided by Penn State University:

Polycystic Ovary Syndrome (PCOS)
Anovulation
Elevated Testosterone

Additional relevant MeSH terms:

Disease
Gonadal Disorders
Physiological Effects of Drugs
Metformin
Endocrine System Diseases
Ovarian Diseases
Cysts
Pharmacologic Actions

Adnexal Diseases
Genital Diseases, Female
Neoplasms
Hypoglycemic Agents
Pathologic Processes
Syndrome
Polycystic Ovary Syndrome
Ovarian Cysts

ClinicalTrials.gov processed this record on February 08, 2010