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NCT00696111
NCT00696111
Who may be able to join
Who might be able to join this trial:
- You have been diagnosed with Polycystic Ovary Syndrome (PCOS)
- You are obese, meaning your Body Mass Index (BMI) is 30 or higher
Who may not be able to join:
- You have been diagnosed with certain hormonal or glandular conditions, such as a specific type of adrenal disorder (nonclassic 21-hydroxylase deficiency), Cushing syndrome, an underactive thyroid, or significantly high levels of a hormone called prolactin
- You have taken steroid medications (including birth control pills), medications that affect how your body handles blood sugar, or medications known to affect sleep, within the 2 months before the study starts
- You are currently pregnant (based on a positive pregnancy test)
- You have been diagnosed with diabetes
- You have high blood pressure (above 140/90 mmHg) that is not well-controlled with either ACE inhibitor or diuretic medications
- You regularly drink alcohol
- You consume more than 300 mg of caffeine per day (roughly 2–3 cups of coffee)
- You have a known allergy to peanuts or to any medications used in this study
- Your blood count is low, specifically if your hemoglobin is below 11 g/dL or your hematocrit is below 33% (confirm with trial site)
- You have a serious ongoing illness affecting your heart, kidneys, liver, or you have been diagnosed with cancer
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Trial details
Status
Completed
Phase
Not Applicable
Sponsor
University of Chicago
Registry
clinicaltrials_gov
Start date
1 December 2007
Est. completion
30 June 2022
Where this trial is recruiting
🇺🇸 United States
Primary endpoints
Estrogen Levels; Sleep Efficiency Measured at Baseline; Total Testosterone
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.