Atlas Trials

A Multinational Study to Evaluate the Effects of a 28-Day Oral Contraceptive on Hemostatic Parameters in Healthy Women

Clinical trial NCT01388491 · COMPLETED

Trial details

NCT number
NCT01388491
Sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Status
COMPLETED
Phase
Phase 2
Study type
INTERVENTIONAL
HemostasisOral Contraceptive
Start date
2011-10-31
Primary completion
2012-09-30
Enrollment
293

View on ClinicalTrials.gov

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