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Postoperative pain relief following caesarean delivery using fascial plane blocks.

Not Applicable
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Registration Number
CTRI/2023/05/053001
Lead Sponsor
I
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

All patients undergoing elective LSCS under spinal anesthesia

Age group: 18- 40years

BMI â?? 18.5 - 30

American society of anaesthesiology (ASA) grade 1 and 2 patients .

Exclusion Criteria

Patient refusal

ASA 3 and above

Patients with features of infection on the anterior abdominal wall

Patients with history of bleeding disorder or on anti coagulant therapy

Patients with known allergy to local anaesthetic drugs

Patients with mental illness or dementia

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Time to requirement of first rescue analgesic dosage <br/ ><br>Timepoint: 0 , 2, 4 , 6 , 12 , 24 hrs
Secondary Outcome Measures
NameTimeMethod
Patient satisfaction score <br/ ><br>Timepoint: 24 hrs;Post operative nausea and vomitingTimepoint: 0 , 2, 4 , 6 , 12 , 24 hrs;VASTimepoint: 0 , 2, 4 , 6 , 12 , 24 hrs
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