Trials / Completed

CompletedNCT01931410

The Effect of Rectal and Sublingual Misoprostol Administration in Postpartum or Intrapartum Haemorrhage at Elective Caesarean Delivery: a Randomized Controlled Trial

Status: Completed
Phase: Phase 4
Study type: Interventional
Enrollment: 618 (actual)

Sponsor: Istanbul Bakirkoy Maternity and Children Diseases Hospital · Other Government
Sex: Female
Age: 18 Years – 44 Years
Healthy volunteers: Not accepted

Summary

The investigators hypothesis in this study is that administration of rectal and sublingual misoprostol decreases intrapartum and postpartum haemorrhage.

Conditions

ıntrapartum Haemorrhage
Postpartum Haemorrhage

Interventions

Type	Name	Description
DRUG	Misoprostol

Timeline

Start date: 2013-06-01
Primary completion: 2014-01-01
Completion: 2014-02-01
First posted: 2013-08-29
Last updated: 2014-02-25

Source: ClinicalTrials.gov record NCT01931410. Inclusion in this directory is not an endorsement.