RecruitingEarly Phase 1NCT06749418
Vascular Effects of High-Salt After Preeclampsia
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
- Anna Stanhewicz, PhD
- Principal Investigator
- Anna Reid-Stanhewicz, PhDUniversity of Iowa
- Intervention
- Eplerenone(drug)
- Enrollment
- 40 target
- Eligibility
- 18-45 years · FEMALE
- Timeline
- 2025 – 2027
Study locations (1)
- University of Iowa, Iowa City, Iowa, 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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