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Completed

NCT Number: NCT00283816

Impact of Metformin in Teens With Polycystic Ovary Syndrome (PCOS) on Oral Contraceptive Therapy

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.

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

metformin

Drug

Metformin 500 mg. tabs 2 tabs BID for duration of study

Other names: Metformin Hydrochloride Tablets, 500 mg., manufacturer: Mylan Pharmaceuticals, Morgantown, WV

oral contraceptive pill

Drug

Yasmin, drospirenone and ethinyl estradiol 28 tablets

1 tab daily for duration of study

Other names: Yasmin 28 tablets, Manufacturer: Berlex, Montville, NJ 07045

Lifestyle Management Program

Behavioral

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

Quality of Life Questionnaire

Behavioral

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

Oral Glucose Tolerance Test

Procedure

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

Blood work

Procedure

Initial and conclusion blood draws include; comprehensive metabolic profile, CBC and platelet,hormonal assessment and lipids.

Abdominal Ultra Sound

Procedure

transabdominal transducer, which contains integrated software for volume calculation will be used to assess ovarian volume.

Performed twice during study, at baseline and conclusion

Dual-energy x-ray absorptiometry (DEXA scan)

Procedure

Dual-energy x-ray absorptiometry (DEXA) will be used to assess percent body fat Performed twice during study, at baseline and conclusion

Placebo

Drug

placebo capsules, two capsules BID

Other names: placebo formulation: 240 mg. lactose powder USP, in size 3 capsules from Capsugel

Primary outcomes

  1. Reduction in Abdominal Fat as Measured by Waist Circumference.

    Time frame: baseline and 24 weeks

    Change in waist circumference measured in cms used as a measure of abdominal adiposity, pre minus post intervention

Secondary outcomes

  1. Change in Weight Post Minus Pre Intervention.

    Time frame: baseline and 24 weeks

    Body mass index change in adolescents enrolled in lifestyle intervention program

  2. Total Testosterone Change

    Time frame: baseline and 24 weeks

    Change in total testosterone post minus pre intervention

  3. Change in Sex Hormone Binding Globulin (SHBG)

    Time frame: baseline and 24 weeks

    SHBG concentration post minus pre-intervention

Sponsors and collaborators

Lead sponsor

University of Rochester

Other

Registry information

Official study title

Metabolic Impact of Oral Contraceptives With or Without Metformin in Obese Adolescents With Polycystic Ovary Syndrome (PCOS)

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Jan 30, 2006
Registry last updated
May 15, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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