Condition: Metabolic Syndrome · Polycystic Ovary Syndrome · Sponsor: University of Pennsylvania
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.
This description comes directly from the study's public registry record.
Anuja Dokras, MD PhD · 215-615-0085 · adokras@pennmedicine.upenn.edu
Andrea Morley · 215-615-4202 · andrea.morley@pennmedicine.upenn.edu
Always discuss trial participation with your own doctor first.
| University of Pennsylvania | Philadelphia, Pennsylvania, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06852365