Trials / Completed
CompletedNCT03401450
Optimal Location of Nerve Block to Minimize Perioperative Opioid Administration in ACL Surgery: Comparing True Adductor Canal to Proximal Block
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 69 (actual)
- Sponsor
- NYU Langone Health · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This is a prospective, randomized, single blinded trial involving human subjects. The goal of this study is to determine an optimal location (proximal or distal) for the nerve block and whether it will make a difference in how much opioid the patient will receive during and after surgery. Ultrasound will identify the adductor canal and the proximal end of the adductor canal/apex of the femoral triangle to determine the location of the blocks. Their will be two randomized groups: 1. ACB within true AC with bupivacaine 0.5% 20cc2. ACB proximal to true AC with bupivacaine 0.5% 20cc
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | ACB within true AC with bupivacaine 0.5% 20cc | The adductor canal block (ACB) is more commonly being used to provide post-operative analgesia since it provides a sensory block with minimal motor block. |
| DRUG | ACB proximal to true AC with bupivacaine 0.5% 20cc | Patients will receive ultra-sound guided single femoral triangle block injection with 20 mL of 0.5% bupivicaine |
Timeline
- Start date
- 2018-02-01
- Primary completion
- 2019-01-25
- Completion
- 2021-06-29
- First posted
- 2018-01-17
- Last updated
- 2023-07-14
- Results posted
- 2020-12-23
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03401450. Inclusion in this directory is not an endorsement.