
Prospective Evaluation of Exparel Adductor Canal Field Block for Pain Control After Anterior Cruciate Ligament Reconstruction
The purpose of this study is to determine if Exparel—a potentially longer lasting version of a local pain killer—can provide a longer period of pain relief and a reduction in opioid pain pill usage following anterior cruciate ligament reconstruction surgery. Patients enrolled in the study will...
About
Protocol Description
Patients enrolled in the study will have a 50/50 chance of receiving either standard bupivacaine (a localized pain killer) or Exparel (our study version of this pain killer) as a block given in the interior thigh (to provide pain relief down the leg). In addition to receiving one of these two medications, all participants will receive a postoperative pain diary in which they will record their daily pill use, and pain scores until their visit at approximately 2 weeks. The diaries will allow us to gather information on day-to-day changes in pill use patterns and pain scores. The pain scales that we will utilize include the numeric pain rating scale (NRS) which is a common measure used in the literature that ranges from 0-10, and an intervention-based pain scale based on medication usage, needs, and how well their current medication regimen is treating their pain.

Eligibility Criteria
Inclusion Criteria
- 18-65 years old
- Isolated, first time ACL reconstruction
- Operation scheduled for Roanoke Ambulatory Surgery Center (RASC)
Exclusion Criteria
- Prior opioid use within 30 days of operation
- Multi-ligament injury
- Allergic to study drugs
- Use of opioids for chronic pain management
- Not medically eligible for surgery
Primary Investigator
Contact Information
Cara Spivey, M.S.
Clinical Research Coordinator
