Last reviewed · How we verify

NCT07448597

Progesterone Preeclampsia

Not yet recruiting Phase 4 Last updated 4 March 2026
What this trial tests

Phase 4 trial testing Progesterone supplementation in Preeclampsia in 642 participants. Not yet recruiting.

Timeline
1 May 2026
Primary endpoint
1 May 2028
1 May 2028

Quick facts

Lead sponsorMedical University of South Carolina
PhasePhase 4
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment642
Start date1 May 2026
Primary completion1 May 2028
Estimated completion1 May 2028

Drugs / interventions tested

Conditions studied

Sponsor

Medical University of South Carolina

Who can join

18 and older, female only, with Preeclampsia or Hypertensive Disorder of Pregnancy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This randomized controlled trial evaluates whether nightly vaginal micronized progesterone (400 mg) initiated before 12 weeks' gestation reduces the incidence of preeclampsia in low-risk pregnant individuals. Participants will be randomly assigned (1:1) to receive either vaginal progesterone through 16 weeks' gestation or routine prenatal care without progesterone. Maternal and neonatal outcomes-including development of preeclampsia, obstetric complications, gestational diabetes, preterm birth, and neonatal morbidity-will be collected via chart review. The study aims to determine whether early progesterone supplementation decreases the risk of preeclampsia.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Progesterone supplementation

Trials testing the same drug.

Other recruiting trials for Preeclampsia

Currently open trials in the same condition.

Other Medical University of South Carolina trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07448597.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing