drugset / Trial / NCT06632379

AtorvaStatin Postpartum and Reduction of Cardiovascular risK

NCT06632379 ↗

Phase 4 Recruiting 76 enrolled Ohio State University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective is to conduct a double-blinded randomized controlled trial of atorvastatin vs. placebo among postpartum individuals with hypertensive disorders of pregnancy, to improve cardiovascular risk score postpartum. For this, 76 individuals with hypertensive disorders of pregnancy (HDP) will be randomized to atorvastatin 10mg or placebo, which will be started in the postpartum period after cessation of breast feeding and continued for 3 months.

Timeline

Start
2025-10-03
Primary completion
2026-09-15
Completion
2026-12-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator Atorvastatin Small molecule 10 mg —

Indications