drugset / Trial / NCT03466333

Postnatal Enalapril to Improve Cardiovascular fUnction Following Preterm Pre-eclampsia

NCT03466333

Phase 2 Completed 118 enrolled Manchester University NHS Foundation Trust
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a double blind randomised controlled feasibility study investigating the effect of postnatal enalapril on cardiovascular function in women who have had preterm pre-eclampsia. Participants will be randomised to 6 months of enalapril or placebo within 3 days of delivery. Cardiovascular function will be assessed using serial echocardiography and biomarkers.

Timeline

Start
2018-09-05
Primary completion
2020-09-11
Completion
2020-09-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Enalapril Other / unclassified 20 mg Oral

Indications