OncoMatch/Clinical Trials/NCT06852365
Combined Oral Contraceptive Pill and Resistance Starch
Is NCT06852365 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Oral Contraceptives, Low-Dose for metabolic syndrome.
Treatment: Oral Contraceptives, Low-Dose — This study will enroll women with PCOS to study the effects of first line therapy, oral contraceptive pills, and then either 12 weeks of resistant starch or 12 weeks of placebo to explore if resistant starch improves cardiometabolic parameters or impacts gut dysbiosis compared to placebo.
Check if I qualifyExtracted eligibility criteria
Lab requirements
Blood counts
hemoglobin >= 10 mg/dl
Kidney function
bun <= 30 mg/dl, serum creatinine <= 1.4 mg/dl
Liver function
ast/alt <= 2x normal, total bilirubin <= 2.5 mg/dl
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- University of Pennsylvania · Philadelphia, Pennsylvania
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