Study ID: DSG-HSP-201
Study Title
- A Multinational Study to Evaluate the Effects of a 28-Day Oral Contraceptive on Hemostatic Parameters in Healthy Women
Teva Identifier
- DSG-HSP-201
ClinicalTrials.gov Identifier
- NCT01388491
Study Status
- Completed
Trial Condition(s)
- Hemostasis | Oral Contraceptive
Interventions
- Drug: desogestrel/ethinyl estradiol and ethinyl estradiol | Drug: desogestrel/ethinyl estradiol
Study Description
- Please refer to ClinicalTrials.gov for a description of the trial
Key Participation Requirements
Gender
- Female
Age Range
- 18 Years to 40 Years
Trial Duration
- 10/01/2011 - 09/01/2012
Phase
- Phase 2
Study Type
Interventional
