Clinical Trials Directory

Trials / Completed

CompletedNCT06086483

Pain Management After Adductor Canal Block for Total Knee Arthroplasty

Pain Management and Functional Recovery After Adductor Canal Block Combined With iPACK Block for Total Knee Arthroplasty. A Prospective, Randomized, Double-blinded Clinical Trial.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
361 (actual)
Sponsor
Poznan University of Medical Sciences · Academic / Other
Sex
All
Age
18 Years – 100 Years
Healthy volunteers
Not accepted

Summary

This randomized, double-blinded, placebo-controlled trial sought to evaluate the efficacy of the iPACK block with Adductor Canal Block on postoperative pain, functional recovery and NLR and PLR levels.

Detailed description

The Interspace between the popliteal artery and capsule of the posterior knee, or iPACK block, together with the Adductor Canal block (ACB), has been described and shows promise in providing analgesia to the knee joint. However, the effect of these two blocks on postoperative pain levels, functional recovery, and stress response is uncertain. This study compares a preoperative iPACK and ACB block to Sham blocks before total knee arthroplasty under spinal anesthesia.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaine 0.2% Injectable Solution20 mL 0.5% ropivacaine was injected into the PENG block 20 mL 0.5% ropivacaine was injected into the Adductor Canal block
DRUG0.9%sodium chloride20 mL 0.9% sodium chloride was injected into the PENG block 20 mL 0.5% sodium chloride was injected into the Adductor Canal block

Timeline

Start date
2020-06-18
Primary completion
2022-07-20
Completion
2023-08-24
First posted
2023-10-17
Last updated
2023-10-17

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT06086483. Inclusion in this directory is not an endorsement.