Study to Evaluate the Safety and Efficacy of Seasonale for Treatment of Low Bone Mineral Density
Withdrawn
Duramed Research
Phase 3
2005-07-01
This is a randomized, multicenter, placebo-controlled study to evaluate the effects of
Seasonale, an extended-regimen oral contraceptive, on bone mineral density in adolescent
females who have had their menstrual period but now have secondary amenorrhea and also have
osteopenia. The duration of the study for each patient will be approximately two years.
A Study to Evaluate Suppression of the Pituitary-Ovarian Axis With Three Different Oral Contraceptive Regimens
Completed
Duramed Research
Phase 3
2005-06-01
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).
Continuous Versus Cyclic Use of Oral Contraceptive Pills in Adolescents
Unknown status
The Physicians' Services Incorporated Foundation
Phase 3
2006-05-01
The primary purpose of this study is to compare the compliance rates of adolescents who take
oral contraceptives (OCPs) continuously to those who take OCPs cyclically.
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