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Clinical Trials/CTRI/2024/07/070260
CTRI/2024/07/070260
Not yet recruiting
Not Applicable

Efficacy of ultrasound guided erector spinae plane block and ultrasound guided oblique sub costal transversus abdominis plane block for postoperative analgesia in laparoscopic cholecystectomy A Comparative Study

Dr Amitesh kumar singh1 site in 1 country38 target enrollmentStarted: July 18, 2024Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Dr Amitesh kumar singh
Enrollment
38
Locations
1
Primary Endpoint
Estimation of total no of doses of 1st rescue analgesic required during first 24 hrs postoperatively

Overview

Brief Summary

This study is a randomized, single blind, parallel group trial comparing the A clinical trial to study analgesic effect of two regional block, Erector spinae plane block and Oblique subcostal transversus abdominis plane block  in patients undergoing laparoscopic cholecystectomy that will be conducted in India. The primary outcome measures will be Estimation of total no of doses of  1st rescue analgesic required during  first 24 hrs postoperatively. The secondary outcomes will be estimation of total duration of block in terms of requirement of 1st rescue analgesia , Mean NRS score at specific time points  postoperatively, Intra operative opioid requirement ,Total number of 2nd  line rescue analgesic dose  required during first  24 hrs postoperatively, Patient satisfaction score -Likert scale (5 point),Documentation of any complications in 1st 24 hrs postoperatively.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 70.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • patients aged 18 yrs to 70yrs scheduled to undergo laparoscopic cholecystectomy patients with ASA I –II.

Exclusion Criteria

  • Patients with bleeding disorders Patients on anticoagulants Pre-existing cardiovascular disease, Hypertension, hepatic and renal failure Advanced psychiatric illness Allergy to local anaesthetics Obesity BMI more than 30.

Outcomes

Primary Outcomes

Estimation of total no of doses of 1st rescue analgesic required during first 24 hrs postoperatively

Time Frame: 24 hrs

Secondary Outcomes

  • 1 estimation of total duration of block in terms of requirement of 1st rescue analgesia(2 Mean NRS score at specific time points postoperatively.)

Investigators

Sponsor
Dr Amitesh kumar singh
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Amitesh kumar singh

Pt. J N M Medical college , Raipur

Study Sites (1)

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