Comparison of ultrasound guided abdominal blocks for postoperative pain relief in adults undergoing elective lower abdominal surgery

Not Applicable

• Conditions: Health Condition 1: O- Medical and Surgical

• Registration Number: CTRI/2023/07/055201
• Lead Sponsor: DEPARTMENT OF ANAESTHESIA

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 25 July 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Patients of ASA status I and II

2.Patients posted for elective lower abdominal surgery under general anaesthesia

Exclusion Criteria

1.Pre-existing coagulation disorders.

2.BMI >30 kg/m2

3.Local infection at the site of block

4.Allergy to Bupivacaine hydrochloride

5.Patients undergoing Laparoscopic lower abdominal surgery

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of post operative analgesiaTimepoint: Duration of post operative analgesia

Secondary Outcome Measures

Name	Time	Method
Total amount of Tramadol consumedTimepoint: in 1st 24 hours;Hemodynamic variations (HR, SBP, DBP, MAP)Timepoint: at 0, 1, 3, 6, 12 & 24 hours <br/ ><br>;Severity of pain using NRS score at rest & movementTimepoint: at 0, 1, 3, 6, 12 & 24 hours