NCT03229057CompletedPhase 3
Comparing the Effects of Oral Contraceptive Pills Versus Metformin
Comparing the Effects of Oral Contraceptive Pills Versus Metformin in the Medical Management of Overweight/Obese Women With Polycystic Ovary Syndrome
Source: ClinicalTrials.gov · Last updated 5 Nov 2025
Brief summary (registry, in English)
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.
- Status (registry)
- Completed
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 240 (actual)
- First submitted
- 13 Jul 2017
- Start date
- 15 Jan 2018
- Primary completion date
- 23 Jan 2024
- Lead sponsor
- Anuja Dokras
- Diseases
- Obesity
- NCT number
- NCT03229057
What you commit to
- Study type: Interventional · Phase 3
- Participants enrolled: 240
- From 15 Jan 2018 to the primary completion date, 23 Jan 2024
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Current use of oral contraceptives, depo progestin, or hormonal implants
- Participation in any study of an investigational drug or device or biological agent within 30 days
- Bariatric surgery procedure in the recent past (\<12 months)
Other illness
- Untreated thyroid disease (TSH \<0.45 mlU/mL and \> 4.5 mlU/mL)
- History of deep venous thrombosis, pulmonary embolus, or cerebrovascular accident
- Current history of alcohol abuse (\>14drinks/week)
- 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
- Patients with a history of, or suspected cervical carcinoma, endometrial carcinoma, or breast carcinoma
- Suspected Cushing's syndrome
- 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.
Lab values
- 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
- Liver disease (AST/ALT\>2 times normal or a total bilirubin \>2.5 mg/dL)
- Renal disease (BUN\>30 mg/dL or serum creatinine \>1.4 mg/dL)
- Anemia (hemoglobin \<10 mg/dL)
Other
- Current pregnancy or desire of pregnancy during course of study
- Currently breastfeeding
- Known 21 hydroxylase deficiency
- Untreated hyperprolactinemia (2 Levels\>30 ng/ml at least one week apart)
- TG\>200mg/dl
- Use of lipid lowering or weight loss agents (subjects may wash out from weight loss agents)
- Suspected adrenal or ovarian tumor secreting androgens
Who the study is looking for
- Women ≥ 18 to ≤ 40 years of age (at the time of screening), with hyperandrogenic PCOS.
- Subjects will be diagnosed with PCOS defined by the most recent Rotterdam criteria based on:
- 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:
- history of chronic anovulation (8 or fewer periods per year)
- AND/OR
- polycystic ovaries.
- BMI ≥ 25 kg/m² to ≤ 48 kg/m² obtained at screening visit.
- In good general health.
- Willing to avoid pregnancy for the duration of the study.
Age in the registry: 18 years to 40 years · Sex: Female · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Penn State Hershey Medical Center Coordinator of this site? Confirm its status | Hershey | United States | Unknown status |
| University of Pennsylvania Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.