Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
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: Active Phase 4 study of Distal Radius Fracture and Dupuytren Contracture, sponsored by St. Luke's Hospital, Pennsylvania.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
our study team contacts the patients 4 days after surgery to ask how long their regional nerve block lasted
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 |
What the registry record for NCT06806410 still lists
NCT06806410 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 241-participant average among 11 other Distal Radius Fracture trials with a reported enrollment target (50% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Distal Radius Fracture
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06806410's enrollment target sits among peer trials
120 5th of 11 higher than 6 of 11 other Distal Radius Fracture trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Distal Radius Fracture trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Perioperative Glucocorticoid Administration in the Treatment of Adult Distal Radius Fractures
RECRUITING · Phase 4
-
Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol for Carpal Tunnel and Distal Radius Fracture Surgeries
COMPLETED · Phase 4
-
Impact of Early ADL Participation on Outcomes Post DRF
RECRUITING · Phase 1
-
Hematoma Block for Distal Radius Fracture
RECRUITING · NA
-
Quantitative and Clinical Assessment of Flexor Tendon Gliding Following Application of a Bioresorbable Hydrogel: A Prospective, Randomized Study in Patients Undergoing Distal Radius Fracture Repair
RECRUITING · NA
-
Go Fit Fast, Recovery Trajectory Using PROMIS®, Linking PROMIS®
ACTIVE NOT RECRUITING
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT01174108 · 120 participants · Phase 2
Allogeneic Hematopoietic Stem Cell Transplantation for Severe Aplastic Anemia and Other Bone Marrow Failure Syndromes Using G-CSF Mobilized CD34+ Selected Hematopoietic Precursor Cells Co-Infused With a Reduced Dose of Non-Mobilized Donor T-cells
- NCT01627301 · 120 participants · NA
Sympathetic Overactivity in Post-traumatic Stress Disorder
- NCT02025023 · 120 participants · Phase 3
Local 5-Fluorouracil Injection for the Treatment of Chalazia: A Prospective, Comparative Study
- NCT02128906 · 120 participants · Phase 2
Radiotherapy With Cisplatin vs. Docetaxel-cetuximab in HNSCC: ERCC1 Biomarker Enrichment and Interaction Design
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI