Clinical trial

Optimizing Preeclampsia Postpartum With Point-of-care Ultrasound

NCT07167862

StatusNOT_YET_RECRUITING

Study typeINTERVENTIONAL

Start date2026-06-15

PhasePHASE4

Study timeline

Study start (estimated)2026-06-15Date precision: day

Registry last updated2026-01-23

Observed by CureCurrent2026-10-07

Recorded dates are source observations, not predictions. Missing milestones are not estimated.

Conditions

Preeclampsiaunresolved

Preeclampsia Postpartumunresolved

Preeclampsia Severe or Mildunresolved

Interventions

Butterfly iQ3 ultrasound system for determination of postpartum volume statusDIAGNOSTIC_TEST

Oral furosemideDRUG

Intravenous furosemideDRUG

Sponsors & collaborators

University of California, Irvinelead sponsor

Mapped research locations

OrangeCalifornia, United States1

Registry source

Open the source record to verify current eligibility, contacts, locations and registry updates.

Open NCT07167862 on ClinicalTrials.gov ↗

Registry-derived research relationships: ClinicalTrials.gov. Raw condition and intervention labels remain distinct from canonical MONDO/RxNorm entities unless separately normalized.