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Clinical Trials/CTRI/2025/08/092600
CTRI/2025/08/092600Not yet recruitingPhase 2/3

Comparison of ultrasound guided femoral triangle block and adductor canal block for postoperative analgesia in total knee arthroplasty

Vardhman Mahavir medical college and Safdarjung hospital1 site in 1 country70 target enrollmentStarted: August 18, 2025Last updated:

Trial Snapshot

Phase
Phase 2/3
Status
Not yet recruiting
Sponsor
Enrollment
70
Locations
1
Primary Endpoint
To compare the analgesic efficacy of ultrasound guided Femoral triangle block and adductor canal block for pain relief using the numerical rating score(NRS) at rest in patients undergoing total knee arthroplasty

Study Overview

Brief Summary

This study is a prospective interventional randomized comparative trial, Comparing the ultrasound guided Femoral triangle block ( 15 ml of 0.25 % bupivacaine and 30 mcg clonidine) and adductor canal block ( 15 ml of 0.25% bupivacaine and 30 mcg clonidine) in patients undergoing total knee arthroplasty under subarachnoid block in a single centre in India. The primary outcome will be measured using Numerical rating score (NRS) postoperatively.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 65.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients aged 18-65 years with American Society of Anesthesiologists physical status I-III scheduled for elective unilateral Total Knee Arthroplasty.

Exclusion Criteria

  • Contraindications to Femoral Triangle and Adductor Canal Block.
  • Patients receiving opioids for chronic analgesic therapy.
  • Contraindication to Subarachnoid Block.
  • Inability to comprehend Numeric Rating Scale.

Outcomes

Primary Outcomes

To compare the analgesic efficacy of ultrasound guided Femoral triangle block and adductor canal block for pain relief using the numerical rating score(NRS) at rest in patients undergoing total knee arthroplasty

Time Frame: At 2 hours postoperatively

Secondary Outcomes

  • NRS at rest(At 0, 1, 4, 8 and 24 hours)
  • NRS on movement(At 24 hours)
  • Time to first rescue analgesia
  • Total analgesic consumption postoperatively(In first 24 hours)
  • Quadriceps muscle strength using Bromage scale(At 24 hours postoperatively)

Investigators

Sponsor
Vardhman Mahavir medical college and Safdarjung hospital
Sponsor Class
Government medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Lohith H T

Vardhman Mahavir medical college and Safdarjung hospital

Study Sites (1)

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