drugset / Trial / NCT03466333
Postnatal Enalapril to Improve Cardiovascular fUnction Following Preterm Pre-eclampsia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Enalapril | Other / unclassified | 20 mg | Oral |