Expired Study
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Temple, Texas 76508


Purpose:

This is a randomized, open-label study to evaluate pituitary ovarian suppression in healthy, reproductive-aged women using three different regimens of oral contraceptives (OCs). Two extended regimen OCs, Seasonale (levonorgestrel/ethinyl estradiol 0.15/0.03 mg for 84 days followed by 7 days of placebo), and Seasonique (levonorgestrel/ethinyl estradiol 0.15/0.03 mg for 84 days followed by 7 days of ethinyl estradiol 0.01 mg), and a 28-day regimen OC, Portia (levonorgestrel/ethinyl estradiol 0.15/0.03 mg for 21 days followed by 7 days of placebo).


Criteria:

Inclusion Criteria: - Premenopausal - Not pregnant or breastfeeding - Weight <200 lbs - Currently taking oral contraceptives in the standard 28-day regimen for at least two months Exclusion Criteria: - Any contraindication to the use of oral contraceptives - Pregnancy within the last 3 months - Smoking > 10 cigarettes per day


NCT ID:

NCT00117273


Primary Contact:

Study Chair
Duramed Protocol Chair
Duramed Research, Inc.


Backup Contact:

N/A


Location Contact:

Temple, Texas 76508
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 12, 2017

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