drugset / Trial / NCT01252186

A Multicenter Study to Evaluate the Effects of a 91-Day Extended Cycle Oral Contraceptive on Hemostatic Parameters in Healthy Women

NCT01252186 ↗

Phase 2 Completed 265 enrolled Teva Women's Health
RandomizedParallel-groupOpen-labelBasic science

Summary

This study is being conducted to evaluate the impact of a 91-day extended cycle oral contraceptive compared to two 28-day oral contraceptive regimens on hemostatic parameters in healthy women.

Timeline

Start
2010-11
Primary completion
2011-12
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator 28-day Desogestrel Oral Contraceptive Unknown 30 ug Oral
Comparator 28-day Levonorgestrel Oral Contraceptive Unknown 30 ug Oral
Comparator Desogestrel Small molecule 150 ug Oral
Comparator Levonorgestrel Small molecule 150 ug Oral
Subject ethinyl estradiol Small molecule 30 ug Oral