Analgesic Efficacy of Different Liposomal Bupivacaine Doses in the Adductor Canal Block for Total Knee Arthroplasty
Recruiting
Phase 3
Interventional Study
Pain, Postoperative
Analgesic Effect
Total Knee Arthroplasty
Liposomal Bupivacaine
Dose Response Relationship, Drug
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Pivotal Trial
This treatment is in the last trial phase before FDA approval.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 – 80
- Sex
- Any
- Trial phase
- Phase 3
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 177 (estimated)
- Sponsor
- The University of Hong Kong · Other
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About This Trial
Total knee arthroplasty is a commonly performed orthopaedic surgery for the treatment of end-stage osteoarthritis when conservative management becomes ineffective. TKA is associated with significant acute postoperative pain and many patients experience severe postoperative pain despite the use of multimodal analgesia. Poor acute postoperative pain control impacts rehabilitation, prolongs recovery …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* ASA I-III
* Age 18-80 years old
* Scheduled for elective primary unilateral total knee arthroplasty (TKA) with robotic surgery
* Able to speak and understand Cantonese or Mandarin or English
* Able to provide informed oral and written consent
Exclusion Criteria:
* Revision T…
Contacts