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Analgesic action in caesarean sectio

Not Applicable
Conditions
Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium
Registration Number
CTRI/2022/01/039421
Lead Sponsor
itin garg
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. parturients between age 18 to 40 years

2. ASA grade II

3. Parturients posted for c section under spinal anaesthesia

4. parturients undergoing c section by pfannenstiel incision

Exclusion Criteria

1. parturients refusal

2. parturients with known sensitivity to drug under evaluation

3. parturients with known systemic disease

4. parturients with complicated pregnancy

5.any contraindication to spinal anaesthesia

6. severe fetal distress

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
primary outcome of study is to determine time for first rescue analgesic demand and total rescue analgesic dose requirement in 24 hoursTimepoint: primary outcome of study is to determine time for first rescue analgesic demand and total rescue analgesic dose requirement in 24 hours
Secondary Outcome Measures
NameTimeMethod
Secondary outcome will be evaluation of ObsQoR-11 score at 24 hour post operatively. <br/ ><br>Timepoint: Secondary outcome will be evaluation of ObsQoR-11 score at 24 hour post operatively. <br/ ><br>
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