Clinical Trials Directory

Trials / Completed

CompletedNCT02292082

The Combination of Adductor Canal Block and Periarticular Injection. A Novel Technique for Patients Undergoing Total Knee Replacement (ACB PAI)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
111 (actual)
Sponsor
Hospital for Special Surgery, New York · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Total knee replacement is associated with severe post-operative pain. The purpose of this study is to compare two methods of treatment for pain control following Total Knee Replacement with an accelerated physical therapy protocol to aid the achievement of rehab milestones.

Detailed description

A total of 106 patients undergoing total knee arthroplasty will be randomized into two groups: one to receive only Periarticular injections and the other periarticular injections AND adductor canal block. Patients will be asked their numeric pain scores before surgery as baseline and at 24 and 48 hours post-operation. Patients also will be asked questions from painOUT questionnaire at 24 and 48 hours. Time to reach discharge criteria based on physical therapy assessments will also be measured.

Conditions

Interventions

TypeNameDescription
DRUGBupivacaine
DRUGMorphine
DRUGMethylprednisolone
DRUGCefazolin
DRUGNormal saline
DRUGMidazolam
DRUGPropofol
DRUGDexamethasone
DEVICE8 MHz. Chiba needle, 22 G / 4 inches

Timeline

Start date
2014-11-01
Primary completion
2016-08-01
Completion
2016-08-01
First posted
2014-11-17
Last updated
2019-01-11
Results posted
2019-01-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02292082. Inclusion in this directory is not an endorsement.