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Clinical Trial Summary

This study is being conducted to evaluate the impact of a 28-day oral contraceptive compared to two 28-day oral contraceptive regimens containing different synthetic progestins on ovarian follicular activity and hormone levels in healthy women.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01291004
Study type Interventional
Source Teva Branded Pharmaceutical Products R&D, Inc.
Contact
Status Completed
Phase Phase 1
Start date January 31, 2011
Completion date March 31, 2012

See also
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