RecruitingPhase 4NCT05139238
Postpartum Hypertension Study
Studying Preeclampsia
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
- Columbia University
- Principal Investigator
- Whitney A. Booker, MDColumbia University
- Intervention
- Labetalol(drug)
- Enrollment
- 104 target
- Eligibility
- 18 years · FEMALE
- Timeline
- 2022 – 2027
Study locations (1)
- Columbia University Irving Medical Center, New York, New York, United States
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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