RecruitingPhase 2NCT02989025

Progesterone to Enhance the Efficacy and Success of Expectantly Managed Preterm Severe/Superimposed Preeclampsia

Studying Preeclampsia

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Key facts

Sponsor
University of Mississippi Medical Center
Principal Investigator
Babbette LaMarca, PhD
University of Missisippi Medical Center
Intervention
17 OHPC(drug)
Enrollment
60 target
Eligibility
18-45 years · FEMALE
Timeline
2017 – 2027

Study locations (1)

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.

Open NCT02989025 on ClinicalTrials.gov

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