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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
University of Rochester
About
Eligibility
Locations
Arms
Outcomes
Full info

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

12 Years - 18 Years (Child, Adult)FemaleAccepts Healthy Volunteers

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

    First Posted
    July 8, 2008
    Last Updated
    April 29, 2015
    Sponsor
    University of Rochester
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    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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