Trials / Completed
CompletedNCT03738696
Liposomal Bupivacaine in Rotator Cuff Repair
Efficacy of Liposomal Bupivacaine in Arthroscopic Rotator Cuff Repair
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 64 (actual)
- Sponsor
- University of Alabama at Birmingham · Academic / Other
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
To assess the efficacy of interscalene liposomal bupivacaine in controlling postoperative pain scores, oral morphine equivalents and sleep quality after arthroscopic rotator cuff repair surgery as compared to interscalene catheter.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Exparel | A long-acting injectable sodium channel blocker bound to lipid that is indicated in controlling postoperative pain |
| DRUG | Ropivacaine | A short-acting injectable sodium channel blocker bound to lipid that is indicated in controlling postoperative pain |
Timeline
- Start date
- 2019-12-15
- Primary completion
- 2022-01-01
- Completion
- 2022-01-01
- First posted
- 2018-11-13
- Last updated
- 2024-05-16
- Results posted
- 2024-05-16
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03738696. Inclusion in this directory is not an endorsement.