- Conditions
- Postpartum Depressive Mood, Postpartum Sexual Function
- Interventions
- Ethinyl Estradiol 35mcg/Norethindrone 1mg, Ethinyl Estradiol 20mcg/Norethindrone 1mg
- Drug
- Lead sponsor
- The Jones Institute
- Other
- Eligibility
- 18 Years to 45 Years · Female only
- Enrollment
- 33 participants
- Healthy volunteers
- Accepts healthy volunteers
- Timeline
- Started 2014
- U.S. locations
- 1
- States / cities
- Norfolk, Virginia
Source: ClinicalTrials.gov public record
Updated Aug 6, 2014 · Synced May 21, 2026, 7:12 PM EDT