Treatment of Adolescent Polycystic Ovary Syndrome (PCOS)
Primary Purpose
Polycystic Ovary Syndrome
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Metformin
Oral Contraceptive Pills (Yasmin)
Lifestyle Modification
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring Polycystic Ovary Syndrome, Overweight Adolescent Girls, Irregular Menstrual Cycles
Eligibility Criteria
Inclusion Criteria:
- Menstrual irregularity defined as cycle length > 45 days
- Overweight as BMI > 25
- Clinical evidence of hirsuitism or acne
- Testosterone > 50ng/dL
Exclusion Criteria:
- History of diabetes mellitus
- History of Cushing's disease
- History of hyperprolactinemia
- Untreated hypo or hyperthyroidism
- History of adrenal hyperplasia
- Significant renal impairment
- Received oral contraceptives, estrogen or progestin or other drugs known to effect lipoprotein metabolism within 2 months of starting the study
- Exercise > 10 hours per week
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Active Comparator
Placebo Comparator
Arm Label
1
2
3
4
Arm Description
Metformin
Oral Contraceptive Pills
lifestyle modification program
placebo to active metformin arm
Outcomes
Primary Outcome Measures
Measure Number of Adolescent Girls With PCOS Who Can be Successfully Recruited Into a Randomized Clinical Trial That Includes Lifestyle Modification
The measure is to determine a number of successfully recruited overweight or obese adolescents to a randomized trial of lifestyle therapy in the community of Rochester, NY
Secondary Outcome Measures
Weight Loss in Lifestyle Intervention Group
In the adolescent women assigned to the lifestyle program, did the intervention program obtain weight reduction as measured by change in BMI
Change in Free Androgen Index (FAI)
Secondary measures of reduction in androgen measures of the different treatment arms. This is a ratio of total testosterone to sex hormone binding globulin (SHBG). The lower values correlate with lower amount of free testosterone. FAI <4 is consistent with a normal range.
Change in SHBG
Measurement of SHBG by treatment group pre and post intervention
Triglyceride Concentration by Treatment Group
Change in triglyceride measures pre and post intervention as representative of lipid changes by treatment group; metformin, lifestyle intervention, oral contraceptive or placebo
Change in Fasting Glucose
Change in fasting glucose concentration by treatment group pre to post intervention
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00714233
Brief Title
Treatment of Adolescent Polycystic Ovary Syndrome (PCOS)
Official Title
Treatment of Polycystic Ovary Syndrome (POS) in Overweight Adolescents
Study Type
Interventional
2. Study Status
Record Verification Date
May 2011
Overall Recruitment Status
Completed
Study Start Date
August 2002 (undefined)
Primary Completion Date
April 2004 (Actual)
Study Completion Date
December 2007 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Rochester
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
A 24 week study to compare the use of Metformin, birth control pills and a carefully planned intensive lifestyle program that includes weight loss and exercise. These approaches will be compared to placebo (a pill that contains no active substances. Metformin, birth control pills and the lifestyle management program will be used on this research study to compare their ability to:
reduce fasting glucose levels
reduce androgen hormone levels
improve sex steroid binding, and
improve lipids (fatty substances in the blood)
Detailed Description
Polycystic ovary syndrome (PCOS) is a condition associated with irregular menstrual cycles, (due to lack of regular ovulation), and evidence of elevated androgen (male hormone) levels, such as unwanted hair growth or acne. This condition often becomes recognized at the time of puberty. The standard treatment for this condition is oral contraceptive pills, which are used not for contraception, but to cause a regular, monthly bleeding pattern.
Many adolescents with PCOS have increased levels of insulin, a hormone that controls the body's sugar balance. These increased insulin levels may play a role in the development of polycystic ovary syndrome. There are several medications now available, which can decrease the insulin levels by improving the action of insulin in the body. Metformin is one of these drugs. Metformin is a drug currently used in the management of diabetes to control blood sugar. It is hoped that by lowering the insulin levels some of the symptoms of polycystic ovary syndrome, such as the lack of regular periods and unwanted hair growth, can be reversed or diminished.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
Polycystic Ovary Syndrome, Overweight Adolescent Girls, Irregular Menstrual Cycles
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
43 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Metformin
Arm Title
2
Arm Type
Experimental
Arm Description
Oral Contraceptive Pills
Arm Title
3
Arm Type
Active Comparator
Arm Description
lifestyle modification program
Arm Title
4
Arm Type
Placebo Comparator
Arm Description
placebo to active metformin arm
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Metformin 425mg. capsules, 2 capsules BID x 24 weeks
Intervention Type
Drug
Intervention Name(s)
Oral Contraceptive Pills (Yasmin)
Other Intervention Name(s)
Yasmin oral COntraceptive tabs
Intervention Description
Yasmin oral contraceptive tabs; 1 tab daily x 24 weeks
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle Modification
Intervention Description
weekly classes x 24 weeks for training in diet, exercise and behavior modification skills
Intervention Type
Drug
Intervention Name(s)
placebo
Other Intervention Name(s)
pharmacy matched placebo capsules
Intervention Description
placebo to the active metformin arm. 2 capsules BID x 24 weeks.
Primary Outcome Measure Information:
Title
Measure Number of Adolescent Girls With PCOS Who Can be Successfully Recruited Into a Randomized Clinical Trial That Includes Lifestyle Modification
Description
The measure is to determine a number of successfully recruited overweight or obese adolescents to a randomized trial of lifestyle therapy in the community of Rochester, NY
Time Frame
24 week
Secondary Outcome Measure Information:
Title
Weight Loss in Lifestyle Intervention Group
Description
In the adolescent women assigned to the lifestyle program, did the intervention program obtain weight reduction as measured by change in BMI
Time Frame
baseline and 24 weeks
Title
Change in Free Androgen Index (FAI)
Description
Secondary measures of reduction in androgen measures of the different treatment arms. This is a ratio of total testosterone to sex hormone binding globulin (SHBG). The lower values correlate with lower amount of free testosterone. FAI <4 is consistent with a normal range.
Time Frame
baseline and 24 weeks
Title
Change in SHBG
Description
Measurement of SHBG by treatment group pre and post intervention
Time Frame
baseline and 24 weeks
Title
Triglyceride Concentration by Treatment Group
Description
Change in triglyceride measures pre and post intervention as representative of lipid changes by treatment group; metformin, lifestyle intervention, oral contraceptive or placebo
Time Frame
baseline and 24 weeks
Title
Change in Fasting Glucose
Description
Change in fasting glucose concentration by treatment group pre to post intervention
Time Frame
baseline and 24 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Menstrual irregularity defined as cycle length > 45 days
Overweight as BMI > 25
Clinical evidence of hirsuitism or acne
Testosterone > 50ng/dL
Exclusion Criteria:
History of diabetes mellitus
History of Cushing's disease
History of hyperprolactinemia
Untreated hypo or hyperthyroidism
History of adrenal hyperplasia
Significant renal impairment
Received oral contraceptives, estrogen or progestin or other drugs known to effect lipoprotein metabolism within 2 months of starting the study
Exercise > 10 hours per week
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathleen M Hoeger, MD
Organizational Affiliation
University of Rochester
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Treatment of Adolescent Polycystic Ovary Syndrome (PCOS)
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