RecruitingPhase 4NCT06665997
Clinical and Biomarker Effects of Depot Medroxyprogesterone Acetate in Females With Sickle Cell Disease
Studying Sickle cell disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Pennsylvania
- Principal Investigator
- Andrea Roe, MD MPH, MD, MPHUniversity of Pennsylvania
- Intervention
- Depot medroxyprogesterone acetate (DMPA)(drug)
- Enrollment
- 65 enrolled
- Eligibility
- 18-50 years · FEMALE
- Timeline
- 2025 – 2027
Study locations (2)
- Emory University, Atlanta, Georgia, United States
- Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
Collaborators
National Heart, Lung, and Blood Institute (NHLBI) · Emory University · Children's Hospital of Philadelphia
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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