Trial intelligence / Profile preview

Misoprostol for Hemorrhage Prevention in Elective Caesarean Delivery

NCT01931410Phase 4Completed

Start
Jun 2013
Primary completion
Jan 2014
Modality
Small Molecules
01

Overview

Phase 4, randomised, double-blind trial of misoprostol in postpartum hemorrhage (PPH) and intrapartum hemorrhage. Primary endpoint: Postpartum Haemorrhage at 24 hours. Started Jun 2013; status: completed.

02

Drugs

misoprostol
03

Conditions

postpartum hemorrhage (PPH)intrapartum hemorrhage

Beyond the preview

Go deeper on NCT01931410.

Study design, results and competitive context are available in the Gosset platform where reported.

Study design & results

Available in the Gosset platform where reported.

Competitive context

Available in the Gosset platform where reported.

Bring the full picture into focus.

See how Gosset can support your research on NCT01931410.

Gosset Free

Get started with Gosset.

Enter your corporate email.

Work email preferred.

Book a call