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Randomised study comparing pre-emptive versus post-operative analgesia at port sites during laparoscopic cholecystectomy

Phase 3
Conditions
Health Condition 1: K802- Calculus of gallbladder without cholecystitis
Registration Number
CTRI/2023/08/056175
Lead Sponsor
All India Institute of Medical SciencesAIIMS New Delhi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.All patients undergoing laparoscopic cholecystectomy for symptomatic gall stone disease.

2.BMI <= 35

3.18 to 65 years of age both male and female

4.Weight > 50 kg

5.Patient is able to follow instructions

6.Able to provide informed written consent

Exclusion Criteria

1.Age > 65 or <18

2.BMI > 35

3.Patient with history of ERCP, Cholecystitis, Pancreatitis

4.Unable to give consent or patient refusal

5.Unfit for general anaesthesia

6.Pregnancy

7.Converted to open

8.Prior upper abdominal surgery

9.Difficult cholecystectomy with operative duration more than 60 minutes

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the average pain score (VAS) between two groupsTimepoint: 1,3,6,12, 24 hrs
Secondary Outcome Measures
NameTimeMethod
To compare the length of hospital stay <br/ ><br>Timepoint: 24, 48 HRS;To compare the time to the first analgesic request (considering time at extubation to be zero) <br/ ><br>Timepoint: 24HRS;To correlate level of intraoperative dissection with post operative pain <br/ ><br>Timepoint: 24HRS
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