Supraclavicular Bupivacaine Vs. Supraclavicular Liposomal Bupivacaine for Orthopedic Wrist Surgery (NCT06179004)
Randomized Controlled Trial of Supraclavicular Bupivacaine Vs. Supraclavicular Liposomal Bupivacaine for Orthopedic Wrist Surgery
๐ฉบ Plain-English Summary (8th-Grade Level)
Orthopedic wrist procedures often cause significant postoperative pain. A supraclavicular nerve block is an effective and proven method to help reduce postoperative pain and decrease opioid use around the time of upper extremity surgery. Liposomal bupivacaine (Exparel) has been approved for use around the brachial plexus, but its analgesic efficacy has limited data. The investigators' goal is to evaluate the effectiveness of Exparel as compared to plain bupivacaine. The investigators hope to ensure the quality of pain control around the time of distal radius fracture repair and reduce the variability of care at the investigators institution by prospectively and rigorously collecting perioperative data during this study.
Who can join: Review the eligibility criteria below.
Location: UNC Chapel Hill โ Chapel Hill, North Carolina
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- UNC Chapel Hill โ Chapel Hill, North Carolina
๐ Contact the Study Coordinator
Phone: (919) 951-5062
Email: jay_schoenherr@med.unc.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Distal Radius Fractures
- Hematoma Block Versus Bier Block for Closed Fracture Reduction โ Salt Lake City, Utah
- ORIF Distal Radius Blood Flow Restriction Therapy โ Houston, Texas
- Topical TRanexamic Acid vs. Placebo on Acute Postoperative Pain Following DRF Fixation โ Toronto, Ontario
- Impact of Early ADL Education on Outcomes Post DRF ORIF โ Washington, Virginia
Explore by condition: All Distal Radius Fractures clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.