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Effect of lignocaine infusion on postoperative pain relief for patients undergoing abdominal hernia surgery.

Not Applicable
Conditions
Health Condition 1: null- asa physical status Iand II
Registration Number
CTRI/2018/04/013168
Lead Sponsor
Sir Gangaram hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

ASA physical status I and II, age more than 18 years, scheduled to undergo laparoscopic IPOM surgery

Exclusion Criteria

age <18 years and > 70 years

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
POSTOPERATIVE PAIN RELIEFTimepoint: VAS SCORE measured at 2, 4,8,12,24 hours
Secondary Outcome Measures
NameTimeMethod
intraoperative hemodynamic stabilityTimepoint: assessment for 24 hrs;length of hospital stayTimepoint: for 24 hrs;patient satisfactionTimepoint: for 24 hrs;perioperative analgesic consumptionTimepoint: for 24 hrs;postoperative nausea and vomitingTimepoint: for 24 hrs;recovery of bowel functionTimepoint: for 24 hrs
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