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Clinical Trials/CTRI/2020/10/028736
CTRI/2020/10/028736
Not yet recruiting
Phase 3

Comparison between preoperative versus postoperative rectal misoprostol in controlling blood loss after cesarean section- a double blind randomized controlled trial.

IPGMER0 sites0 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: O72- Postpartum hemorrhage
Sponsor
IPGMER
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
IPGMER

Eligibility Criteria

Inclusion Criteria

  • Pregnant women at term who are electively prepared for caesarean section under regional anaesthesia.

Exclusion Criteria

  • Antepartum haemorrhage, maternal hypertension, coagulation disorder, previous 2 or more caesarean section, multiple gestation, fetal macrosomia, polyhydramnios, previous uterine rupture, hypersensitivity to prostaglandin.

Outcomes

Primary Outcomes

Not specified

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