Clinical Trials Directory

Trials / Completed

CompletedNCT03703206

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

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

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
120 (actual)
Sponsor
University of Pennsylvania · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

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).

Conditions

Interventions

TypeNameDescription
DRUGultrasound guided injection of local anesthetic between the popliteal artery and the capsule of the knee (iPACK)nerve block for posterior knee pain after a TKA.

Timeline

Start date
2018-07-01
Primary completion
2019-08-27
Completion
2021-08-27
First posted
2018-10-11
Last updated
2024-05-30
Results posted
2024-05-30

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03703206. Inclusion in this directory is not an endorsement.

The Analgesic Efficacy of Protocol for Primary Total Knee Arthroplasty (TKA) (NCT03703206) · Clinical Trials Directory