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The Analgesic Efficacy of Protocol for Primary Total Knee Arthroplasty (TKA)

Knee Arthroplasty, Total Clinical Trial

Official title:
The Analgesic Efficacy of Adding the IPACK Block to a Multimodal Analgesia Protocol for Primary Total Knee Arthroplasty

Clinical Trial Summary

This is a perspective, randomized, blinded study with a parallel design and an allocation ratio of 1 to 1 for the treatment groups to assess the analgesic efficacy of adding the iPACK (injection between the popliteal artery and the capsule of the knee) in addition to the adductor canal block (ACB) for Total Knee Arthoplasty patients (TKA).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03703206
Study type Interventional
Source University of Pennsylvania
Contact
Status Completed
Phase Phase 3
Start date July 1, 2018
Completion date August 27, 2021
View Details
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