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Diclofenac Patch vs inj paracetamol Following Cesarean Delivery

Not Applicable
Conditions
Health Condition 1: - Health Condition 2: O82- Encounter for cesarean delivery without indication
Registration Number
CTRI/2020/11/029204
Lead Sponsor
Armed Forces Medical College Pune
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

ll women undergoing elective caesarean delivery at term with singleton pregnancy

Exclusion Criteria

Emergency caesarean delivery

Preterm caesarean delivery

Intraoperative complication

Postpartum hemorrhage

NSAID allergy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measurement for the intensity of pain postoperatively at 6, 12, 18 and 24 hours by visual analogue scale (VAS) of 0 -10 points.Timepoint: Measurement for the intensity of pain postoperatively at 6, 12, 18 and 24 hours by visual analogue scale (VAS) of 0 -10 points.
Secondary Outcome Measures
NameTimeMethod
Secondary end point <br/ ><br>Number of times rescue analgesic required. <br/ ><br>Timepoint: 6hrs <br/ ><br>12hrs <br/ ><br>18hrs <br/ ><br>24hrs
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