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Clinical Trials/CTRI/2025/09/094356
CTRI/2025/09/094356
Not yet recruiting
Not Applicable

A Comparison Between Adductor Canal Block and Femoral Nerve Block for Postoperative Analgesia in Patients Undergoing Total Knee Replacement

SRMS IMS1 site in 1 country68 target enrollmentStarted: August 10, 2027Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
SRMS IMS
Enrollment
68
Locations
1
Primary Endpoint
To compare visual analogue scale (VAS) scores at different period of time in postoperative period between Adductor canal block group and Femoral nerve block group.

Overview

Brief Summary

Knee replacement surgery is often followed by significant pain, which can slow recovery and limit early movement. Nerve blocks are commonly used to reduce this pain. The Femoral Nerve Block has been used for many years but may cause weakness in the thigh muscles, affecting walking after surgery. The Adductor Canal Block is a newer method that provides good pain relief while better preserving muscle strength.

This study aims to compare these two techniques in patients undergoing knee replacement surgery. The objective is to find out which block gives better pain relief, fewer side effects, and faster return of mobility after the operation.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

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

Inclusion Criteria

  • Patients aged 18-70 years of either sex ASA physical status I/II/III.

Exclusion Criteria

  • ASA physical status IV Contraindications to spinal anaesthesia Pregnancy Major psychiatric diseases and history of substance abuse Hypersensitivity to study drug- Bupivacaine hydrochloride 0.5% Patient refusal.

Outcomes

Primary Outcomes

To compare visual analogue scale (VAS) scores at different period of time in postoperative period between Adductor canal block group and Femoral nerve block group.

Time Frame: The patients will be assessed for pain using visual analogue scale (VAS) score and mobility by observing the angle of flexion of knee joint at 1, 2, 3, 6, 12, 24 and 48 hours in the postoperative period.

To compare range of motion in knee joint as angle of flexion upto 48 hours in the two groups

Time Frame: The patients will be assessed for pain using visual analogue scale (VAS) score and mobility by observing the angle of flexion of knee joint at 1, 2, 3, 6, 12, 24 and 48 hours in the postoperative period.

Secondary Outcomes

  • To compare opioid consumption in the two groups in first 48 hours

Investigators

Sponsor
SRMS IMS
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Aakash Kasana

Department of Anaesthesia, Shri Ram Murti Smarak Institute of Medical Sciences (SRMS IMS)

Study Sites (1)

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