Low Dose OC Therapy in Women With Polycystic Ovary Syndrome (PCOS): Impact of BMI on Hyperandrogenism
Sponsored by Woman's
About this trial
Last updated 8 years ago
Study ID
RP 11-003
Status
Completed
Type
Interventional
Phase
Phase 4
Placebo
No
Accepting
16 to 35 Years
Female
Not accepting
Healthy Volunteers
Trial Timing
Ended 10 years ago
What is this trial about?
The classic description of polycystic ovary syndrome (PCOS) is that it is a disorder
characterized by menstrual irregularity, chronic anovulation, androgen excess, and
abnormal gonadotropin secretion. Use of combined oral contraceptives (OCs) in women with
PCOS effectively reduces circulating androgens. Although OCs are the most common and one
of the oldest symptomatic treatment modalities for androgenic skin symptoms and for
irregular menstrual cycles caused by hyperandrogenism, the data concerning the effect of
treatment of PCOS women with different body mass index (BMI) are limited. This study is
being done to compare the hormone and metabolic changes after treatment with low-dose
oral birth control regimen of DRSP 3 mg/EE 0.02mg/levomefolate calcium 0.451 mg (Beyaz™)
in women with PCOS with different body weights.
What are the participation requirements?
Inclusion Criteria
- •Adult female-16 years to 35 years of age who have been diagnosed with PCOS desiring contraception
- Actual BMI >18 to <35kg/ m2
- Written consent for participation in the study
- Patient completed lactation
Exclusion Criteria
- Metabolic abnormalities requiring pharmacological intervention (except controlled thyroid disease)
- Uncontrolled hypertension
- Cancer or history of hormone-dependent cancer
- History of cholestasis
- Presence of contradictions for OC administration
- Personal history of cardiovascular events.
- Use of drugs known to exacerbate glucose tolerance.
- No prescription or over-the-counter weight-loss drugs
- Diabetes
- Use of medications that affect blood pressure or lipid profile
- Smoking in past 6 months
- Known thrombogenic mutations (e.g. Factor V Leiden)
- Current or history of deep venous thrombosis/pulmonary embolism
- Major surgery with prolonged immobilization
- Injectable hormonal contraceptive use within 6 months
- Use of hormonal (e.g., oral contraceptive [OC] pill) or insulin-sensitizing medication unless willing to cease medications for 3 months before study measurements