Trials / Completed
CompletedNCT02604550
Anterior Cruciate Ligament Pain Study
Comparison Between Femoral Nerve Block and Adductor Canal Block for Anterior Cruciate Ligament Reconstruction: A Prospective Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 115 (actual)
- Sponsor
- Emory University · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to compare the pain control benefit of two different types of nerve blocks in patients undergoing anterior cruciate ligament (ACL) reconstruction.
Detailed description
This trial is a prospective, randomized, surgeon-blinded, two-armed trial to investigate the safety and efficacy of femoral nerve blocks versus adductor canal blocks for participants undergoing outpatient anterior cruciate ligament (ACL) reconstruction surgery. The objective of this study is to compare the pain control benefit of two different types of nerve blocks. Ropivacaine, which is FDA-approved for use in both femoral nerve blocks as well as adductor canal blocks, will be utilized. The study will be comparing the efficacy between FDA approved treatments.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ropivacaine 0.5% | Ropivacaine 0.5% will be administered to the femoral nerve or adductor canal. |
| DRUG | Percocet 7.5/325 | Percocet 7.5/325 will taken as needed up to every four hours. |
| DRUG | Naprosyn 500 mg | Naprosyn 500 mg will be taken twice daily. |
Timeline
- Start date
- 2015-11-01
- Primary completion
- 2016-04-01
- Completion
- 2016-04-01
- First posted
- 2015-11-13
- Last updated
- 2017-05-31
- Results posted
- 2017-05-31
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02604550. Inclusion in this directory is not an endorsement.