Clinical trial · Interventional
Low Dose OC Therapy in Women With Polycystic Ovary Syndrome (PCOS): Impact of BMI on Hyperandrogenism
Positive Clinical and Hormonal Effects of Ethinylestradiol Combined With Drospirenone (EE/DRSP) in Women With Polycystic Ovary Syndrome (PCOS): Impact of Body Weight and Relevance to Hyperandrogenism
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Polycystic Ovary Syndrome | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 3 mg DRSP/20 μg EE | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- 3 mg DRSP/20 μg EE--normal weight
- description
- Folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive Normal weight -BMI 18-24.9 kg/ m2
- interventionNames
- Drug: 3 mg DRSP/20 μg EE
- type
- EXPERIMENTAL
- label
- 3 mg DRSP/20 μg EE- Overweight
- description
- Folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive BMI 25-29.9 kg/ m2
- interventionNames
- Drug: 3 mg DRSP/20 μg EE
- type
- EXPERIMENTAL
- label
- 3 mg DRSP/20 μg EE- Grade 1 obese
- description
- Folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive BMI 30-34.9 kg/ m2
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 16 Years
- Maximum age
- 35 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available