drugset / Trial / NCT07293728

A Randomized Feasibility Trial Comparing Drospirenone and Norethindrone for Postpartum Hypertension Management in Preeclampsia

NCT07293728

Phase 4 Not yet recruiting 50 enrolled Oregon Health and Science University
RandomizedParallel-groupOpen-labelTreatment

Summary

This is an open-label, randomized feasibility trial in which patients admitted to Oregon Health \& Science University (OHSU) after a pregnancy complicated by preeclampsia who are considering a progestin-only pill contraception postpartum will be randomized to norethindrone or drospirenone for 6 weeks following hospital discharge.

Timeline

Start
2026-07
Primary completion
2026-12
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Norethindrone Unknown 0.35 mg
Subject drospirenone Unknown 4 mg

Indications