A randomised, double-blind, placebo-controlled, flexible-dose, parallel-group study to evaluate the efficacy, safety and toleration of oral sildenafil citrate administered in the dose range of 20-80 Mg TID [three times daily] for the treatment of pre-eclampsia (PET)

Status: Discontinued

Phase of Trial: Phase II

Latest Information Update: 02 Feb 2021

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At a glance

Drugs Sildenafil (Primary)
Indications Preeclampsia
Focus Therapeutic Use
Sponsors Pfizer

Most Recent Events

01 Nov 2009 Results published in Hypertension in Pregnancy.
08 Jun 2007 Status changed from in progress to discontinued.
02 Feb 2007 Status change from recruiting to in progress

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