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Clinical Trials/CTRI/2025/04/085965
CTRI/2025/04/085965
Not yet recruiting
Not Applicable

Comparison of Analgesic Efficacy between ultrasound guided quadratus lumborum block and landmark guided caudal block in paediatric patients undergoing unilateral lower abdominal surgeries

Dr Udipta Bhuyan1 site in 1 country100 target enrollmentStarted: May 15, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Dr Udipta Bhuyan
Enrollment
100
Locations
1
Primary Endpoint
To compare the analgesic requirement in the first 24 hours

Overview

Brief Summary

Paediatric patients undergoing lower abdominal surgeries often experience postoperative pain, necessitating effective analgesia to optimise recovery and discomfort.

Inadequate analgesia in the paediatric patients can cause biobehavioural changes that may modulate future responses to pain .

Providing adequate analgesia is a pre-requisite for early and enhanced recovery after surgery.

Quadratus lumborum block and caudal block are regional anaesthesia techniques used to provide postoperative pain relief in this population.

Hence, this study aims to compare the analgesic requirements in the first 24 hours postoperatively between Quadratus lumborum block and caudal block in paediatric patients undergoing unilateral lower abdominal surgeries.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
1.00 Year(s) to 8.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Aged 1-8 years 2.ASA Grade 1 and 2 3.Scheduled for unilateral lower abdominal surgery under general anaesthesia.

Exclusion Criteria

  • 1.Parent of the patient not willing to give consent.
  • 2.Allergy to the study drug 3.Infection at the site of block 4.Spinal deformity 5.Developmental delay 6.Seizure disorder 7.Disorders of coagulation 8.Cardiovascular,renal and liver diseases.

Outcomes

Primary Outcomes

To compare the analgesic requirement in the first 24 hours

Time Frame: Postoperative pain will be assessed by using the FLACC scale at 30mins,1,2,4,6,12 and 24 hours

Secondary Outcomes

  • 1.Duration of analgesia between the two groups(2.Pain scores between the two groups)

Investigators

Sponsor
Dr Udipta Bhuyan
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Udipta Bhuyan

Gauhati Medical College and Hospital

Study Sites (1)

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