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Clinical Trials/CTRI/2025/04/083775
CTRI/2025/04/083775
Not yet recruiting
Not Applicable

Effects of Adductor canal block combined with infiltration between the popliteal artery and capsule of the knee on pain management compared with epidural analgesia for patients undergoing total knee arthroplasty a randomised controlled trial

Armed Forces Medical College Pune1 site in 1 country78 target enrollmentStarted: April 1, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Armed Forces Medical College Pune
Enrollment
78
Locations
1
Primary Endpoint
to compare the visual analogue scale VAS of the patients at postoperative 8th hour during passive physical therapy movements

Overview

Brief Summary

Total knee arthroplasty is regarded as one of the most painful orthopaedic operations. Adequate pain relief is essential in the immediate postoperative period to enable ambulation, initiation of physiotherapy, prevention of postoperative complications. A variety of procedures are currently being employed to achieve the same including neuraxial anaesthesia and regional anaesthesia including Adductor canal block. However, ACB does not relieve posterior knee pain and hence the addition of IPACK block ( infiltration between popliteal artery and capsule of the knee) has shown promising results in providing significant posterior knee analgesia without affecting motor nerves resulting in better range of motion and ambulation compared to adductor canal block alone

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 90.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • ASA grade 1 to 3 body mass indexes between 18 to 40 kg/m2 fully oriented and cooperative.

Exclusion Criteria

  • refusal to participate any contraindication to neuraxial anaesthesia lower extremity neuropathy local anaesthetic allergy revision surgery advanced liver, heart, kidney failure inability to comprehend VAS score cognitive impairment.

Outcomes

Primary Outcomes

to compare the visual analogue scale VAS of the patients at postoperative 8th hour during passive physical therapy movements

Time Frame: VAS of the patients at postoperative 8th hour during passive physical therapy movements

Secondary Outcomes

  • to compare VAS score of the patients at 1st postoperative day and 2nd postoperative day during active and passive physical therapy movements

Investigators

Sponsor
Armed Forces Medical College Pune
Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Manjot Multani

Armed forces medical college,

Study Sites (1)

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