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To compare the postoperative pain relief in laparoscopic cholecystectomy by bilateral transverse abdominal plane block and giving the drug intraperitoneal along with skin infiltration.

Not Applicable
Conditions
Health Condition 1: K800- Calculus of gallbladder with acutecholecystitis
Registration Number
CTRI/2022/06/043353
Lead Sponsor
SRM Medical College Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients with ASA Physical Status I and II posted for laparoscopic cholecystectomy

2.Weighing between 50 â?? 100 kg

Exclusion Criteria

1.All patients with ASA Physical Status III and above

2.Patients who refuse to participate in the study

3.Patients who are allergic to amide local anaesthetics

4.Patients who are pregnant

5.Patients with chronic cardiac, renal or hepatic condition

6.Patients with coagulation abnormalities

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To estimate the duration of postoperative analgesiaTimepoint: patient is assessed for pain second hourly using Visual Analogue Scale for 24 hours
Secondary Outcome Measures
NameTimeMethod
1.To estimate the Consumption of morphine in 24 hour postoperative period <br/ ><br>2.Intraoperative consumption of opioids <br/ ><br> <br/ ><br>Timepoint: second hourly monitoring is done for 24 hours
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