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NCT05086224 · ClinicalTrials.gov registry record · Early Phase 1
Hematoma Block Versus Bier Block for Closed Fracture Reduction
A Early Phase 1 study of Distal Radius Fractures, sponsored by University of Utah.
- Active
- Registry status
- Early Phase 1
- Development phase
- 500
- Enrollment target
- 1
- Study location
NCT05086224: Active Early Phase 1 study of Distal Radius Fractures, sponsored by University of Utah.
NCT05086224 is a Early Phase 1 study of Distal Radius Fractures that is active but no longer recruiting, run by University of Utah. The registered enrollment target is 500 participants, above the 71-participant average among 4 other Distal Radius Fractures trials with a reported enrollment target (604% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05086224, a Early Phase 1 study of Distal Radius Fractures, is active but no longer recruiting, sponsored by University of Utah.
- ACTIVE NOT RECRUITING
- Registry status
- Early Phase 1
- Development phase
- 500 participants
- Enrollment target
- 1
- Study location
Study Summary
The investigators objective of this study is to evaluate the effectiveness of hematoma block versus intravenous regional anesthesia (Bier block) during closed reduction of distal radius fractures.
Primary Outcome
VAS pain score (0 no pain - 10 severe pain)
Conditions Studied
Interventions
- DRUG Hematoma Local Anesthetic Block Procedure with 1% Lidocaine
- DRUG Bier Anesthetic Block Procedure with 1% Lidocaine
Study Locations (1)
Utah
- University of Utah Orthopaedic Center - Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 500 participants |
| Start Date | 2021-07-15 |
| Est. Completion | 2025-07 |
| Phase | Early Phase 1 |
What the registry record for NCT05086224 still lists
NCT05086224 is an interventional study that assigns participants to a tested intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap, above the 71-participant average among 4 other Distal Radius Fractures trials with a reported enrollment target (604% higher).
The record links to 1 condition, with Distal Radius Fractures appearing as the primary indexed condition, and to 2 interventions - of which Hematoma Local Anesthetic Block Procedure with 1% Lidocaine is the first listed.
NCT05086224 reports a single indexed study location in Utah.
Frequently Asked Questions
What is clinical trial NCT05086224 about?
NCT05086224 is a clinical study titled "Hematoma Block Versus Bier Block for Closed Fracture Reduction". The investigators objective of this study is to evaluate the effectiveness of hematoma block versus intravenous regional anesthesia (Bier block) during closed reduction of distal radius fractures.
What is the current status of trial NCT05086224?
This trial is currently active not recruiting. It is a Early Phase 1 study. The enrollment target is 500 participants. The study started on 2021-07-15. Estimated completion is 2025-07.
What conditions does trial NCT05086224 study?
This clinical trial studies the following conditions: Distal Radius Fractures.
What interventions are being tested in trial NCT05086224?
The interventions under investigation include: Hematoma Local Anesthetic Block Procedure with 1% Lidocaine (DRUG), Bier Anesthetic Block Procedure with 1% Lidocaine (DRUG).
Who is sponsoring clinical trial NCT05086224?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05086224 being conducted?
This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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