The Effect of Metformin Added to Clomiphene Citrate on Pregnancy Rates in Hyperandrogenic, Chronic Oligoovulatory or Anovulatory Women
Information source: Wilford Hall Medical Center
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Polycystic Ovary Syndrome; Anovulation; Oligoovulation; Infertility; Hyperandrogenism
Intervention: Metformin (Drug); Clomiphene citrate (Drug); Placebo (Drug)
Phase: Phase 3
Status: Completed
Sponsored by: Wilford Hall Medical Center Official(s) and/or principal investigator(s): Randal D Robinson, MD, Principal Investigator, Affiliation: Wilford Hall Medical Center and Brooke Army Medical Center
Summary
The purpose of our study was to conduct a placebo controlled, double-blind randomized trial
in chronic oligoovulatory or anovulatory , hyperandrogenic, infertility patients comparing
the effects of adjuvant metformin plus clomiphene citrate to clomiphene citrate plus placebo
on pregnancy rates and ovulation rates. We hypothesized that combining metformin with
clomiphene citrate would result in higher ovulation and pregnancy rates in hyperandrogenic
women who have chronic oligoovulation or anovulation as the sole etiology for their
infertility and who have unknown responsiveness to clomiphene citrate.
Clinical Details
Official title: The Effect of Metformin Added to Clomiphene Citrate on Pregnancy Rates in Hyperandrogenic, Chronic Oligoovulatory or Anovulatory Women: A Randomized Trial
Study design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Primary outcome: Pregnancy RatesOvulation Rates
Secondary outcome: Pregnancy Outcome
Detailed description:
Women with polycystic ovary syndrome (PCOS), defined as chronic oligoovulation or anovulation
and hyperandrogenism, are primarily treated with clomiphene citrate as first line therapy if
they desire pregnancy. However, women with PCOS have lower than expected pregnancy rates in
response to clomiphene citrate. Approximately 20% of women with PCOS are resistant to
clomiphene citrate. Subjects with chronic oligoovulation or anovulation and hyperandrogenism
will ovulate 80% of the time, but pregnancy occurs in only 40%. The ideal initial treatment
regimen for women with PCOS who desire pregnancy has not been determined.
Metformin (Glucophage; Bristol-Myers Squibb, Princeton, NJ) is an insulin sensitizer and
lowers serum insulin and androgen levels. Numerous case studies, case series, retrospective
studies, and non-placebo controlled prospective studies, have suggested an improvement in
insulin sensitivity, spontaneous menses, ovulatory response and pregnancies when metformin
was given alone or prior to initiation of ovulation inducing agents in women with chronic
anovulation and hyperandrogenism.
However, there has been conflicting evidence in the literature regarding the effect of
metformin alone or in combination with ovulation inducing agents regarding ovulation and
pregnancy rates in prospective, randomized trials. Therefore, it remains unknown if the use
of metformin plus clomiphene citrate in non-selected, infertility patients with PCOS improves
ovulation and pregnancy rates compared to the use of clomiphene citrate alone.
Women with a history of infertility and diagnosed with hyperandrogenic, oligoovulatory or
anovulatory cycles as the sole etiology for their infertility were randomized to receive
clomiphene citrate 50 mg days 5-9, plus metformin 500 mg three times daily versus clomiphene
plus placebo. The dose of clomiphene was increased up to a maximum dose of 250 mg in a
step-wise fashion until ovulation was confirmed with an ovulation predictor kit. Once
ovulation was confirmed the subjects continued the ovulatory dose of clomiphene for 6
ovulatory cycles or until conception. Metformin or placebo was started on cycle day one and
discontinued 8 days after the LH surge and/or by cycle day 21. A positive HCG, ovulation
rates and pregnancy outcome were the outcome measures.
Eligibility
Minimum age: 18 Years.
Maximum age: 40 Years.
Gender(s): Female.
Criteria:
Inclusion Criteria:
- Married
- Hyperandrogenic women 18-40 years old who desired fertility and who demonstrated
chronic anovulation or oligoovulation
- Had patent fallopian tubes and whose partners had normal semen analyses were eligible
for enrollment in the study.
Exclusion Criteria:
- Androgen secreting tumours
- Diabetes mellitus
- Thyroid abnormalities
- Hyperprolactinemia
- Adult onset congenital adrenal hyperplasia
- Diminished ovarian reserve
- Subjects who used hormonal medications two months prior to the start of the trial.
Locations and Contacts
Wiford Hall Medical Center, Lackland AFB, Texas 78236, United States
Additional Information
Starting date: December 1997
Ending date: April 2003
Last updated: December 18, 2006
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