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NCT02346929 · ClinicalTrials.gov registry record · NA
Hematoma Block for Distal Radius Fracture
A NA study of Distal Radius Fracture, sponsored by Beth Israel Deaconess Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 115
- Enrollment target
- 1
- Study location
NCT02346929: Recruiting NA study of Distal Radius Fracture, sponsored by Beth Israel Deaconess Medical Center.
NCT02346929 is a NA study of Distal Radius Fracture that is actively recruiting participants, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 115 participants, below the 242-participant average among 11 other Distal Radius Fracture trials with a reported enrollment target (52% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02346929, a NA study of Distal Radius Fracture, is actively recruiting participants, sponsored by Beth Israel Deaconess Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 115 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine the efficacy of ultrasound guided hematoma block versus traditional "blind" hematoma block for analgesia in distal radius fracture reduction.
Primary Outcome
Subjects will be surveyed on a Visual Analog Scale (VAS) on their pain during 4 points: prior to receiving hematoma block, after receiving hematoma block, during reduction and prior to discharge
Conditions Studied
Interventions
- OTHER ultrasound guide
Study Locations (1)
Massachusetts
- Beth Israel Deaconess Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 115 participants |
| Start Date | 2014-08 |
| Est. Completion | 2027-12 |
| Phase | NA |
What NCT02346929 shows while recruiting
NCT02346929 is an interventional study that assigns participants to a tested intervention. The registered 115 participants enrollment target is mid-sized for trials with a published cap, below the 242-participant average among 11 other Distal Radius Fracture trials with a reported enrollment target (52% lower).
The record links to 1 condition, with Distal Radius Fracture appearing as the primary indexed condition, and to 1 intervention - of which ultrasound guide is the first listed.
NCT02346929 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT02346929 about?
NCT02346929 is a clinical study titled "Hematoma Block for Distal Radius Fracture". The purpose of this study is to determine the efficacy of ultrasound guided hematoma block versus traditional "blind" hematoma block for analgesia in distal radius fracture reduction.
What is the current status of trial NCT02346929?
This trial is currently recruiting. It is a NA study. The enrollment target is 115 participants. The study started on 2014-08. Estimated completion is 2027-12.
What conditions does trial NCT02346929 study?
This clinical trial studies the following conditions: Distal Radius Fracture.
What interventions are being tested in trial NCT02346929?
The interventions under investigation include: ultrasound guide (OTHER).
Who is sponsoring clinical trial NCT02346929?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02346929 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT02346929's enrollment target sits among peer trials
115 7th of 11 higher than 5 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
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