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A clinical trial to study the effect of two drugs oxytocin and carbetocin in management of third stage of labour in vaginal deliveries

Phase 3
Conditions
Health Condition 1: O720- Third-stage hemorrhage
Registration Number
CTRI/2024/05/066832
Lead Sponsor
Rajendra institute of medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All women undergoing vaginal delivery

Exclusion Criteria

Women who undergo caesarean section

Women with proven hypersensitivity to oxytocin and carbetocin

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postpartum haemorrhage more than 500 ml blood lossTimepoint: Postpartum haemorrhage more than 500 ml blood loss
Secondary Outcome Measures
NameTimeMethod
eed for blood Transfusion and fall in hemoglobin levelsTimepoint: Hemoglobin fall more than 1 gm/dl
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