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Active Not RecruitingNCT06806410

The Efficacy of Liposomal Bupivacaine in Ultrasound Guided Supraclavicular Nerve Blocks for Hand and Wrist Surgery

The Efficacy of Liposomal Bupivacaine in Ultrasound Guided Supraclavicular Nerve Blocks for Hand and Wrist Surgery: a Prospective, Randomized, Blinded Controlled Trial

Status
Active Not Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
St. Luke's Hospital, Pennsylvania · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Patients undergoing hand, wrist, and elbow surgery may experience pain after surgery. The orthopedic surgeon may provide prescription pain medications after surgery to assist with pain control. However, with concern of the opioid epidemic, many patients would rather minimize the use of narcotic pain prescriptions after having surgery. As an alternative, ultrasound guided regional nerve blocks can assist with postoperative pain control. patients consented to this study will be randomized into three groups: 1) will receive an ultrasound guided nerve block with local anesthesia only, 2) will receive an ultrasound guided nerve block with local anesthesia and a steroid dexamethasone, 3) will receive an ultrasound guided nerve block with liposomal bupivacaine. our study team will make phone calls after surgery to the patient to determine how long the block lasted for, and how many opioid pain pills were taken up to 3 days after surgery.

Detailed description

Our study team predicts that the ultrasound guided nerve block with liposomal bupivacaine can last approximately 48 hours, while the block with local anesthesia and dexamethasone will last approximately 30 hours, and the block with local anesthesia only may last up to 24 hours

Conditions

Interventions

TypeNameDescription
DRUGLiposomal bupivacaine (LB)our study team wishes to determine effect of liposomal bupivacaine in regional nerve blocks for surgery of the upper extremity (finger, hand, wrist, elbow)
DRUGDexamethasonedexamethasone injected in perineural area can extend the regional nerve block

Timeline

Start date
2023-05-01
Primary completion
2024-11-30
Completion
2025-01-30
First posted
2025-02-04
Last updated
2025-02-06

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06806410. Inclusion in this directory is not an endorsement.