Atlas Trials

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

Clinical trial NCT01252186 · COMPLETED

Trial details

NCT number
NCT01252186
Sponsor
Teva Women's Health
Status
COMPLETED
Phase
Phase 2
Study type
INTERVENTIONAL
HemostasisOral Contraceptive
Start date
2010-11-01
Primary completion
2011-12-01
Enrollment
265

View on ClinicalTrials.gov

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