Clinical Trials Directory

Trials / Completed

CompletedNCT03038425

Does Continuous Adductor Canal Nerve Block Improve the Quality of Recovery for Outpatient Total Knee Arthroplasty Patients?

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
81 (actual)
Sponsor
Ottawa Hospital Research Institute · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This is a randomized, double-blinded pilot study to determine whether patients undergoing ambulatory total knee arthroplasty (TKA) using a subvastus approach benefit from the addition of a continuous adductor canal nerve block (cACB) catheter along with an existing multimodal approach to postoperative analgesia. Outcomes include the 15-item Quality of Recovery Scale (QoR-15) (Miles 2016), pain scores, opioid consumption, opioid-free days, functional outcome as measured by the Time Up and Go (TUG) test, patient satisfaction, patient's rating of catheter effectiveness, and complications.

Conditions

Interventions

TypeNameDescription
DRUGNormal SalineThis is the placebo intervention - normal saline infused in the adductor canal via a catheter. There are no anticipated therapeutic effect
DRUGRopivacaineThis is the treatment intervention - ropivacaine 0.2% infused in the adductor canal via a catheter. This will provide analgesia to the knee after TKA

Timeline

Start date
2017-05-02
Primary completion
2020-04-01
Completion
2020-04-01
First posted
2017-01-31
Last updated
2020-12-22

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03038425. Inclusion in this directory is not an endorsement.