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NCT06806410 · ClinicalTrials.gov registry record · Phase 4
The Efficacy of Liposomal Bupivacaine in Ultrasound Guided Supraclavicular Nerve Blocks for Hand and Wrist Surgery
A Phase 4 study of Distal Radius Fracture and Dupuytren Contracture, sponsored by St. Luke's Hospital, Pennsylvania.
- Active
- Registry status
- Phase 4
- Development phase
- 120
- Enrollment target
- 1
- Study location
NCT06806410 is a Phase 4 study of Distal Radius Fracture and Dupuytren Contracture that is active but no longer recruiting, run by St. Luke's Hospital, Pennsylvania. The registered enrollment target is 120 participants, below the 241-participant average among 11 other Distal Radius Fracture trials with a reported enrollment target (50% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06806410, a Phase 4 study of Distal Radius Fracture and Dupuytren Contracture, is active but no longer recruiting, sponsored by St. Luke's Hospital, Pennsylvania.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 4
- Development phase
- 120 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- DRUG Dexamethasone
- DRUG Liposomal bupivacaine (LB)
Study Locations (1)
Pennsylvania
- St. Luke's University Health Network - Bethlehem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2023-05-01 |
| Est. Completion | 2025-01-30 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06806410
The ClinicalTrials.gov registry entry for NCT06806410 describes a study currently listed as active not recruiting, categorized as Phase 4. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 241-participant average among 11 other Distal Radius Fracture trials with a reported enrollment target (50% lower). The listed sponsor is St. Luke's Hospital, Pennsylvania, which has 10 total studies on file at ClinicalTrials.gov.
The record links to 8 conditions, with Distal Radius Fracture appearing as the primary indexed condition, and to 2 interventions - of which Dexamethasone is the first listed.
NCT06806410 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT06806410 about?
NCT06806410 is a clinical study titled "The Efficacy of Liposomal Bupivacaine in Ultrasound Guided Supraclavicular Nerve Blocks for Hand and Wrist Surgery". 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...
What is the current status of trial NCT06806410?
This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 120 participants. The study started on 2023-05-01. Estimated completion is 2025-01-30.
What conditions does trial NCT06806410 study?
This clinical trial studies the following conditions: Distal Radius Fracture, Dupuytren Contracture, Hand Surgery, Wrist Surgery, Elbow Surgery.
What interventions are being tested in trial NCT06806410?
The interventions under investigation include: Dexamethasone (DRUG), Liposomal bupivacaine (LB) (DRUG).
Who is sponsoring clinical trial NCT06806410?
This trial is sponsored by St. Luke's Hospital, Pennsylvania, which has 10 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06806410 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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