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oxytocin vs oxytocin & methylergometrine in controlling intrapartum cesarean sectio

Phase 2
Registration Number
CTRI/2023/07/055548
Lead Sponsor
AIIMS Jodhpur
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

pregnant women 18 years and above

laboring patients who undergo a cesarean section

Exclusion Criteria

placental / uterine abnormalities

chronic HTN , Gestational HTN, Preeclampsia

HIV/AIDS on protease inhibitors

history of Coronary heart disease

history of hypersensitivity to methylergometrine

underlying uncorrected structural heart disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the effectiveness of multimodal prophylactic uterotonic x 24 hours post deliveryTimepoint: INTRAOPERATIVELY
Secondary Outcome Measures
NameTimeMethod
blood loss estimation <br/ ><br>hb fall post cesarean <br/ ><br>uterine tone assessment <br/ ><br>patient requiring blood transfusionTimepoint: blood loss ( 2 hours ) <br/ ><br>hb fall post cesarean (24 hours) <br/ ><br>uterine tone assessment (4 mins ) <br/ ><br>patient requiring blood transfusion( till the day of discharge )
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