drugset / Trial / NCT04764916
Evaluation of Exparel Adductor Canal Field Block for Pain Control After ACL Reconstruction
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This is a prospective, randomized study for adult patients presenting to the Carilion Clinic Institute of Orthopedics and Neurosurgery. Patients undergoing isolated ACL reconstruction will be eligible for inclusion. All patients will receive an adductor canal block (either with bupivacaine or Exparel. Patients will be given a pain diary for self-report of pill counts, pain scores, block duration, and pain control satisfaction). Pill counts and pain scores will also be taken by a team member at two and six-week post-operative visits. Primary outcomes include opioid requirements and pain scores.
Timeline
- Start
- 2021-02-16
- Primary completion
- 2022-02-16
- Completion
- 2022-03-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bupivacaine | Other / unclassified | 10 ml | Other |
| Subject | Bupivacaine | Other / unclassified | 20 ml | Other |
Indications
No indication recorded.