Enhanced Recovery After Major Surgery and Chronic Pain for Total Knee Arthroplasty
Recruiting
N/A
Interventional Study
Chronic Pain
Opioid Use
Adductor Canal Block
Total Knee Arthroplasty
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 75
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 64 (estimated)
- Sponsor
- Hospital for Special Surgery, New York · Other
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About This Trial
The goal of this interventional clinical trial is to assess opioid consumption 24-48 hrs post anesthesia block among patients undergoing total knee arthroplasty. The main question it aims to answer is:
1\. Is there a difference in opioid consumption 24-48 hours post block administration among patients that receive an adductor canal catheter (ACC) versus adductor canal block (ACB)?
Participants w…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients with osteoarthritis scheduled for a primary total knee arthroplasty with a participating surgeon
* Age 18 to 75 years
* Planned use of regional anesthesia
* Ability to follow study protocol
* English speaking (secondary outcomes include questionnaires validated in Eng…
Contacts