Overview
Comparing the Effects of Oral Contraceptive Pills Versus Metformin
Status:
Recruiting
Recruiting
Trial end date:
2023-04-30
2023-04-30
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
To determine the effect of Oral Contraceptive Pills (OCP) verses Metformin verses OCP and Metformin on the prevalence of Metabolic Syndrome (MetS) and its components in overweight/obese women with Polycystic Ovary Syndrome (PCOS). The combination of OCP and metformin (OCP, through lowering androgens, and metformin, through improvement in insulin sensitivity) will affect the prevalence of MetS, thereby altering the risk profile for the development of diabetes and possible cardiovascular disease (CVD) in young women with PCOS.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Anuja Dokras
University of PennsylvaniaCollaborators:
Milton S. Hershey Medical Center
National Institutes of Health (NIH)Treatments:
Contraceptive Agents
Contraceptives, Oral
Contraceptives, Oral, Combined
Medroxyprogesterone
Medroxyprogesterone Acetate
Metformin
Criteria
Inclusion Criteria:1. Women ≥ 18 to ≤ 40 years of age (at the time of screening), with hyperandrogenic PCOS.
2. Subjects will be diagnosed with PCOS defined by the most recent Rotterdam criteria
based on:
1. androgen excess (defined as an elevated serum T level or hirsutism, based on a
Ferriman Gallwey score > 8 (note: > 2 for women of Asian descent)
AND either:
2. history of chronic anovulation (8 or fewer periods per year)
AND/OR
3. polycystic ovaries.
3. BMI ≥ 25 kg/m² to ≤ 48 kg/m² obtained at screening visit.
4. In good general health.
5. Willing to avoid pregnancy for the duration of the study.
Exclusion Criteria:
1. Current pregnancy or desire of pregnancy during course of study
2. Currently breastfeeding
3. Known 21 hydroxylase deficiency
4. Untreated thyroid disease (TSH <0.45 mlU/mL and > 4.5 mlU/mL)
5. Untreated hyperprolactinemia (2 Levels>30 ng/ml at least one week apart)
6. Type 1 or type 2 Diabetes Mellitus (elevated fasting serum glucose >126mg/dL on two
occasions, poorly controlled diabetes (HgbA1C>6.5%), currently receiving anti-diabetic
agents, or currently receiving metformin for treatment of diabetes
7. Liver disease (AST/ALT>2 times normal or a total bilirubin >2.5 mg/dL)
8. Renal disease (BUN>30 mg/dL or serum creatinine >1.4 mg/dL)
9. Anemia (hemoglobin <10 mg/dL)
10. History of deep venous thrombosis, pulmonary embolus, or cerebrovascular accident
11. Current history of alcohol abuse (>14drinks/week)
12. Poorly controlled hypertension defined as average systolic blood pressure >= 150 mm Hg
or average diastolic >=100 mm Hg obtained on three measurements obtained 5 minutes
apart. If treated, average systolic blood pressure >=140 mm Hg or average diastolic
>=90 mm Hg
13. Patients with a history of, or suspected cervical carcinoma, endometrial carcinoma, or
breast carcinoma
14. TG>200mg/dl
15. Use of lipid lowering or weight loss agents (subjects may wash out from weight loss
agents)
16. Current use of oral contraceptives, depo progestin, or hormonal implants
17. Participation in any study of an investigational drug or device or biological agent
within 30 days
18. Suspected adrenal or ovarian tumor secreting androgens
19. Suspected Cushing's syndrome
20. Bariatric surgery procedure in the recent past (<12 months)
21. Absolute contraindications to the use of hormonal contraceptives or metformin,
23. Subjects who are unable to comply with the study procedures, for instance due to mental
illness, substance abuse, or participation in other studies.