Randomized Study of the Effect of Decreased Hyperinsulinemia on the Ovulatory Response to Clomiph… (NCT00005654) | Clinical Trial Compass
CompletedNot Applicable
Randomized Study of the Effect of Decreased Hyperinsulinemia on the Ovulatory Response to Clomiphene Citrate in Obese Women With Polycystic Ovary Syndrome
88 participantsStarted 2000-01
Plain-language summary
OBJECTIVES:
I. Determine whether reduction of serum insulin levels by metformin increases ovulatory response to clomiphene or spontaneous ovulation in obese women with polycystic ovary syndrome.
Who can participate
Age range18 Years – 40 Years
SexFEMALE
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PROTOCOL ENTRY CRITERIA:
--Disease Characteristics--
Obese women with chronic anovulation due to polycystic ovary syndrome (PCOS)
Must have oligoamenorrhea and hyperandrogenemia
--Prior/Concurrent Therapy--
At least 2 months since prior standard therapy (including over the counter drugs) At least 2 months since prior investigational agents
--Patient Characteristics--
Hematopoietic: Hematocrit greater than 38%
Hepatic: Liver function normal No clinically significant hepatic disease
Renal: No clinically significant renal disease Creatinine less than 1.4 mg/dL No proteinuria
Cardiovascular: No clinically significant cardiac disease
Pulmonary: No clinically significant pulmonary disease
Hormonal: Thyroid function normal Prolactin normal Fasting 17 alpha-hydroxy progesterone less than 200 mg/dL OR No late onset adrenal hyperplasia 21 alpha-hydroxylase deficiency
Other: Not pregnant Negative pregnancy test Fertile patients must use effective contraception No diabetes mellitus No clinically significant neurologic, psychiatric, infectious, neoplastic, or metabolic disease No clinically significant malignant disease except nonmelanomatous skin cancer At least 1 year since any prior drug abuse or alcoholism
Trial details
NCT IDNCT00005654
SponsorNational Center for Research Resources (NCRR)