Trials / Unknown
UnknownNCT04047745
Post-operative Exparel Study Following Rotator Cuff Repair
The Use of Liposomal Bupivacaine Interscalene Brachial Plexus Block for Rotator Cuff Surgery: A Randomized, Double Blind, Clinical Trial
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 132 (estimated)
- Sponsor
- Rothman Institute Orthopaedics · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary purpose of this study is to determine if the postoperative oral narcotics consumption in patients receiving liposomal bupivacaine (LB) interscalene brachial plexus nerve block (ISBPB) is different than the narcotics consumption receiving traditional bupivacaine ISBPB for arthroscopic rotator cuff repair analgesia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Liposomal bupivacaine | interscalene nerve block administered before surgery using 133 mg liposomal bupivacaine with 10mL 0.5% ropivacaine |
| DRUG | Ropivacaine injection | interscale nerve block administered before surgery using 30mL 0.5% ropivacaine |
Timeline
- Start date
- 2019-09-01
- Primary completion
- 2021-09-01
- Completion
- 2021-09-01
- First posted
- 2019-08-07
- Last updated
- 2019-08-07
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT04047745. Inclusion in this directory is not an endorsement.