Impact of Metformin in Teens With Polycystic Ovary Syndrome (PCOS) on Oral Contraceptive Therapy
Primary Purpose
Polycystic Ovary Syndrome
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Metformin
Oral Contraceptive Pill
Lifestyle Management Program
Quality of Life Questionnaire
Oral Glucose Tolerance Test
Blood work
Abdominal Ultra Sound
Dual-energy x-ray absorptiometry (DEXA scan)
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:Age 12-18 years; Menstrual irregularity; Overweight; Must be able to swallow capsules; At lease 6 months since onset of first menstrual cycle. Exclusion Criteria:Diabetes; Kidney or Liver disease; Tobacco use; Depression or Bipolar Disease; Contraindication to exercise; Weight > 300 lbs.
Sites / Locations
- University of Rochester Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
1
0
Arm Description
metformin
placebo
Outcomes
Primary Outcome Measures
Reduction in Abdominal Fat as Measured by Waist Circumference.
Change in waist circumference measured in cms used as a measure of abdominal adiposity, pre minus post intervention
Secondary Outcome Measures
Change in Weight Post Minus Pre Intervention.
Body mass index change in adolescents enrolled in lifestyle intervention program
Total Testosterone Change
Change in total testosterone post minus pre intervention
Change in Sex Hormone Binding Globulin (SHBG)
SHBG concentration post minus pre-intervention
Full Information
NCT ID
NCT00283816
First Posted
January 27, 2006
Last Updated
April 28, 2015
Sponsor
University of Rochester
1. Study Identification
Unique Protocol Identification Number
NCT00283816
Brief Title
Impact of Metformin in Teens With Polycystic Ovary Syndrome (PCOS) on Oral Contraceptive Therapy
Official Title
Metabolic Impact of Oral Contraceptives With or Without Metformin in Obese Adolescents With Polycystic Ovary Syndrome (PCOS)
Study Type
Interventional
2. Study Status
Record Verification Date
April 2011
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
January 2008 (Actual)
Study Completion Date
January 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Rochester
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Oral contraceptives are known to improve menstrual cycles and symptoms in PCOS, however may increase cholesterol. Metformin, a drug to improve insulin resistance, may benefit metabolic state. This study is to determine whether metformin added to oral contraceptive therapy in adolescent women with PCOS improves metabolic state.The study will also test a lifestyle improvement program to reduce weight.
Detailed Description
Polycystic Ovary Syndrome (PCOS) is a heterogeneous condition characterized by chronic anovulation and androgen excess that occurs in 4-8% of unselected adult women. Although signs and symptoms of the disorder typically appear at the time of puberty, diagnosis is often delayed until adulthood. At least 50% of adult women with PCOS are obese, resulting in a more severe clinical picture. Obesity among adolescents has been increasing in recent years, with overrepresentation of females who show evidence of hyperandrogenism and irregular periods, suggesting an association of obesity and PCOS at an early age. Recent data, however, have drawn attention to the long-term risks of PCOS, including diabetes and cardiovascular disease. Insulin resistance plays a critical role in the pathophysiology of PCOS and is thought to be the metabolic abnormality most closely linked to an increased risk of diabetes and heart disease. Traditional treatments with oral contraceptives are associated with reduction in serum androgens and improvements in menstrual cycles in adolescents with PCOS, however these have not been well-studied in obese adolescents. Oral contraceptives may worsen the dyslipidemia seen in obese women with PCOS and do not address the insulin resistance. Metformin, an insulin sensitizing agent, has been shown to improve metabolic features of PCOS, but combination therapy with oral contraceptives has never been studied in the obese adolescent with PCOS.
The major hypothesis of this proposal is that metformin will improve the metabolic profile of obese adolescent girls with PCOS treated with oral contraceptives. Additionally, a secondary hypothesis will be that compliance with a concurrent lifestyle modification program with be associated with the most significant improvements.
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
ParticipantInvestigator
Allocation
Randomized
Enrollment
36 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
metformin
Arm Title
0
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Metformin Hydrochloride Tablets, 500 mg., manufacturer: Mylan Pharmaceuticals, Morgantown, WV
Intervention Description
Metformin 500 mg. tabs 2 tabs BID for duration of study
Intervention Type
Drug
Intervention Name(s)
Oral Contraceptive Pill
Other Intervention Name(s)
Yasmin 28 tablets, Manufacturer: Berlex, Montville, NJ 07045
Intervention Description
Yasmin, drospirenone and ethinyl estradiol 28 tablets
1 tab daily for duration of study
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle Management Program
Intervention Description
Subjects and a parent/guardian will participate in a series of classes for training in diet, exercise & behavior modification skills on a regular weekly basis over the 24 week study
Intervention Type
Behavioral
Intervention Name(s)
Quality of Life Questionnaire
Intervention Description
Quality of Life questionnaire designed for women with Polycystic Ovary Syndrome. Questions concern health and health related issues Performed twice during study, at baseline and conclusion
Intervention Type
Procedure
Intervention Name(s)
Oral Glucose Tolerance Test
Intervention Description
Insulin response to a glucose challenge in an oral glucose tolerance test (OGTT), as measured by area under the curve (AUC). In this study we will administer an OGTT and calculate the AUC as a measure of insulin resistance.
Performed twice during study, at baseline and conclusion
Intervention Type
Procedure
Intervention Name(s)
Blood work
Intervention Description
Initial and conclusion blood draws include; comprehensive metabolic profile, CBC and platelet,hormonal assessment and lipids.
Intervention Type
Procedure
Intervention Name(s)
Abdominal Ultra Sound
Intervention Description
transabdominal transducer, which contains integrated software for volume calculation will be used to assess ovarian volume.
Performed twice during study, at baseline and conclusion
Intervention Type
Procedure
Intervention Name(s)
Dual-energy x-ray absorptiometry (DEXA scan)
Intervention Description
Dual-energy x-ray absorptiometry (DEXA) will be used to assess percent body fat Performed twice during study, at baseline and conclusion
Intervention Type
Drug
Intervention Name(s)
placebo
Other Intervention Name(s)
placebo formulation: 240 mg. lactose powder USP, in size 3 capsules from Capsugel
Intervention Description
placebo capsules, two capsules BID
Primary Outcome Measure Information:
Title
Reduction in Abdominal Fat as Measured by Waist Circumference.
Description
Change in waist circumference measured in cms used as a measure of abdominal adiposity, pre minus post intervention
Time Frame
baseline and 24 weeks
Secondary Outcome Measure Information:
Title
Change in Weight Post Minus Pre Intervention.
Description
Body mass index change in adolescents enrolled in lifestyle intervention program
Time Frame
baseline and 24 weeks
Title
Total Testosterone Change
Description
Change in total testosterone post minus pre intervention
Time Frame
baseline and 24 weeks
Title
Change in Sex Hormone Binding Globulin (SHBG)
Description
SHBG concentration post minus pre-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:Age 12-18 years; Menstrual irregularity; Overweight; Must be able to swallow capsules; At lease 6 months since onset of first menstrual cycle.
Exclusion Criteria:Diabetes; Kidney or Liver disease; Tobacco use; Depression or Bipolar Disease; Contraindication to exercise; Weight > 300 lbs.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathleen Hoeger, MD
Organizational Affiliation
University of Rochester
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Rochester Medical Center
City
Rochester
State/Province
New York
ZIP/Postal Code
14642
Country
United States
12. IPD Sharing Statement
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Impact of Metformin in Teens With Polycystic Ovary Syndrome (PCOS) on Oral Contraceptive Therapy
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