Comparison of ultrasound guided blocks with local infiltration for pain relief in post operative patients undergoing laparoscopic cholecystectomy.

Phase 3

Not yet recruiting

• Conditions: Medical and Surgical,

• Registration Number: CTRI/2023/04/052035
• Lead Sponsor: Vardhaman Mahavir medical college and Safdarjung hospital

Brief Summary

This study is a prospective, interventional randomised comparitive study conducted in the Department of Anaesthesiology and intensive care, VMMC and Safdarjung hospital to compare the analgesic efficacy of combined External oblique intercostal and rectus sheath block with local infilteration of analgesia at port site for post operative analgesia in ASA grade I and II patients undergoing laparoscopic cholecystectomy with the hypothesis that combined External oblique intercostal and rectus sheath block is superior to local infilteration of analgesia at port site. Primarily post operative VAS score will be recorded at 1 hour. Secondarily, VAS at 2, 4, 6, 8, 12 and 24 will be recorded along with cummulative 24 hour analgesia requirement and time to first rescue analgesia.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2023-04-26
• Study Start: 2023-10-05

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

ASA status I and II undergoing laparoscopic cholecystectomy under general anaesthesia.

Exclusion Criteria

• history of allergy or hypersensitivity to local anaesthetics 2.
• contraindications to block 3.
• inability to understand pain scale.
• BMI > 30 kg/m2 5.
• Pregnancy 6.
• pulmonary, Cardiac, Hepatic and renal diseases.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
to compare the analgesic efficacy of combined External Oblique intercostal and Rectus Sheath block with loacl infilteration of analgesia at port site for post operative analgesia in patients undergoing laparoscopic cholecystectomy.	1 hour post operatively

Secondary Outcome Measures

Name	Time	Method
1. compare and evaluate VAS at 2,4,6,8,12 and 24 hours.	2. time to rescue analgesia.

Trial Locations

Locations (1)

Safdarjung hospital; 🇮🇳 Delhi, DELHI, India

Safdarjung hospital

🇮🇳Delhi, DELHI, India

Vaishnovi Gangadhar

Principal investigator

7259303000

dr.vaishnovi@gmail.com