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
| Type | Name | Description |
|---|---|---|
| DRUG | Normal Saline | This is the placebo intervention - normal saline infused in the adductor canal via a catheter. There are no anticipated therapeutic effect |
| DRUG | Ropivacaine | This 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.