Clinical Trials Directory

Trials / Completed

CompletedNCT01788215

Effect of a Commonly Used Antibiotic, Doxycycline, in Women With Polycystic Ovarian Syndrome

The Use of an MMP Inhibitor, Doxycycline, to Reduce Ovarian Androgen Production and Restore Normal Cycling in Women With Polycystic Ovarian Syndrome

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
10 (actual)
Sponsor
University of Rochester · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to study the effect of a commonly used antibiotic, doxycycline, on the production of ovarian hormones and menstrual cycles in women with Polycystic Ovarian Syndrome (PCOS).

Detailed description

Polycystic ovarian syndrome (PCOS) is one of the leading causes of female infertility, affecting 5-10% of reproductive-age women . This heterogeneous disorder is characterized by anovulatory infertility, androgen excess, an increase in the ratio of LH to FSH, and morphologic polycystic changes to the ovaries. Obesity and insulin resistance are also metabolic factors associated with PCOS that further increase the morbidity in these patients. Inducing fertility in patients with PCOS can be a challenge, as it most often involves ovulation induction that can lead to ovarian enlargement, hyperstimulation, and multiple-birth pregnancies. This study is designed to determine novel effective strategies to promote normal cycling in this patient population.

Conditions

Interventions

TypeNameDescription
DRUGdoxycycline200mg/day in divided doses of 100mg twice daily
OTHERSugar Pill1 pill twice a day

Timeline

Start date
2010-11-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2013-02-11
Last updated
2016-01-13
Results posted
2016-01-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01788215. Inclusion in this directory is not an endorsement.

Effect of a Commonly Used Antibiotic, Doxycycline, in Women With Polycystic Ovarian Syndrome (NCT01788215) · Clinical Trials Directory