Trials / Withdrawn
WithdrawnNCT02426164
Liposomal Bupivacaine in Total Knee Arthroplasty
Analgesic Efficacy of Liposomal Bupivacaine in Total Knee Arthroplasty
- Status
- Withdrawn
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Miller Orthopedic Specialists · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
Liposomal bupivacaine is a novel local anesthetic designed for prolonged pain relief. Despite its long-acting analgesic potential, liposomal bupivacaine is significantly more expensive than other local anesthetic alternatives. The primary aim of this investigation is to examine whether or not liposomal bupivacaine provides superior pain relief or clinically significant opioid-sparing effects versus a control to justify its cost.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Liposomal bupivacaine | Periarticular infiltration of the liposomal bupivacaine with 20cc of normal saline |
| DRUG | bupivacaine HCl, morphine, epinephrine, methylprednisolone | Periarticular infiltration of 24c of bupivacaine HCl, 0.8cc morphine, 0.3cc epinephrine, and 1cc of methylprednisolone |
Timeline
- Start date
- 2015-06-01
- Primary completion
- 2017-06-01
- Completion
- 2017-06-01
- First posted
- 2015-04-24
- Last updated
- 2016-03-22
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02426164. Inclusion in this directory is not an endorsement.