Trials / Completed
CompletedNCT05190120
Adductor Canal Block Versus Femoral Block on Pain and Quadriceps Strength
Effects of Ultrasound-guided Adductor Canal Block Versus Femoral Nerve Block on Pain and Quadriceps Strength After Ambulatory Knee Arthroscopic Surgery
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 132 (actual)
- Sponsor
- University of California, San Francisco · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the effects of a femoral nerve block vs. an adductor canal block on pain and quadriceps muscle strength for knee arthroscopy surgery.
Detailed description
Patients undergoing arthroscopic knee surgery (ACL and non-ACL surgery) typically receive an ultrasound-guided femoral nerve block or an adductor canal block in the pre-operative phase for post-operative pain control. While an effective method for post-operative analgesia, the femoral nerve block is associated with profound quadriceps weakness for the duration of the nerve block, which can impair ambulation, rehabilitation, and increase the risk of falls. The more distal adductor canal block, however, contains primarily sensory branches of the femoral nerve and has been been purported by small volunteer studies to provide equally effective analgesia with minimal motor block and quadriceps weakness (as compared to femoral nerve block). The investigators will prospectively randomize patients undergoing knee arthroscopy at the UCSF Orthopaedic Institute to receive either a single-shot femoral nerve or adductor canal block pre-operatively after taking baseline measurements of quadriceps strength (quantified by maximum voluntary isometric contraction). The quadriceps muscle strength will be checked 20 minutes after the nerve block to assess strength. All patients will subsequently undergo a general anesthetic. The primary outcome variable will be post-block quadriceps strength as a percentage of baseline from pre-block values. Secondary outcome variables that will also investigated include: VAS pain score in the post anesthesia recovery unit and post-operative day 1, duration of nerve blockade, and perioperative opioid consumption.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Femoral Nerve Block | Patients having ACL reconstruction, meniscus surgery and knee arthroscopy |
| PROCEDURE | Adductor Canal Nerve Block | Patients having ACL reconstruction, meniscus surgery and knee arthroscopy |
| DRUG | preoperative Femoral Nerve Block using 20ml of 0.5% ropivacaine | |
| DRUG | Preoperative Adductor canal block with 0.75%% ropivacaine 13.3ml. |
Timeline
- Start date
- 2016-01-01
- Primary completion
- 2022-03-20
- Completion
- 2022-03-20
- First posted
- 2022-01-13
- Last updated
- 2025-09-30
- Results posted
- 2025-09-30
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05190120. Inclusion in this directory is not an endorsement.