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Comparison of two drugs intravenous paracetamol versus intramuscular tramadol for painless delivery

Not Applicable
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Registration Number
CTRI/2019/05/019244
Lead Sponsor
Monisha
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Full term singleton live pregnancy with vertex presentation in active phase of labor. Active phase of labor is described as cervical dilatation of more than or equal to 3cm with good uterine contractions.

Exclusion Criteria

Women with medical disorders, previously scarred uterus, clinical evidence of cephalopelvic disproportion, malpresentation, multiple pregnancy, preterm labor, intrauterine growth restriction, antepartum haemorrhage, pregnancy induced hypertension, gestational diabetes mellitus, foetal distress, history of allergic to any medications, patient presenting for first time in active labor are all excluded from the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
For effective painless deliveryTimepoint: 0min <br/ ><br>30 mins <br/ ><br>60mins <br/ ><br>120mins <br/ ><br>180mins <br/ ><br>240mins <br/ ><br>60min post partum <br/ ><br>120min postpartum <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
For effective painless deliveryTimepoint: 0min <br/ ><br>30 mins <br/ ><br>60mins <br/ ><br>120mins <br/ ><br>180mins <br/ ><br>240mins <br/ ><br>60min post partum <br/ ><br>120min postpartum <br/ ><br>
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