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NCT01808183 · ClinicalTrials.gov registry record
Pediatric Supracondylar Humerus Fracture NIRS Study
A clinical trial of Supracondylar Humerus Fracture, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- 90
- Enrollment target
- 1
- Study location
NCT01808183: Completed study of Supracondylar Humerus Fracture, sponsored by Wake Forest University Health Sciences.
NCT01808183 is a study of Supracondylar Humerus Fracture that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 90 participants, below the 158-participant average among 3 other Supracondylar Humerus Fracture trials with a reported enrollment target (43% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01808183, a study of Supracondylar Humerus Fracture, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- 90 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to use a device to compare the blood flow in the patient's injured arm to the patient's uninjured arm. This will help us determine 'normal' readings for this device for a child's forearm and may in the future help us detect children that have injured the blood vessels that go to the forearm when they have an elbow fracture. The patient will be one of approximately 100 people involved in this research project at Carolinas Medical Center, and the patient's participation will last until the patient is discharged from the hospital. It is hypothesized that if the blood vessel is uninjured, the readings on the NIRS device on the injured arm will be equal to the uninjured arm. It is also hypothesized that if the blood vessel of the injured arm is injured, the readings on the NIRS device will be different than on the uninjured arm.
Conditions Studied
Interventions
- DEVICE Near Infrared Spectroscopy Pads
Study Locations (1)
North Carolina
- Carolinas HealthCare System: Levine Children's Hospital - Charlotte
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2012-02 |
| Est. Completion | 2017-02 |
What the finished NCT01808183 record still lists
NCT01808183 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 158-participant average among 3 other Supracondylar Humerus Fracture trials with a reported enrollment target (43% lower).
The record links to 1 condition, with Supracondylar Humerus Fracture appearing as the primary indexed condition, and to 1 intervention - of which Near Infrared Spectroscopy Pads is the first listed.
NCT01808183 reports a single indexed study location in North Carolina.
Frequently Asked Questions
What is clinical trial NCT01808183 about?
NCT01808183 is a clinical study titled "Pediatric Supracondylar Humerus Fracture NIRS Study". The purpose of this study is to use a device to compare the blood flow in the patient's injured arm to the patient's uninjured arm. This will help us determine 'normal' readings for this device for a child's forearm and may in the future help us detect children that have injured the blood vessels th...
What is the current status of trial NCT01808183?
This trial is currently completed. The enrollment target is 90 participants. The study started on 2012-02. Estimated completion is 2017-02.
What conditions does trial NCT01808183 study?
This clinical trial studies the following conditions: Supracondylar Humerus Fracture.
What interventions are being tested in trial NCT01808183?
The interventions under investigation include: Near Infrared Spectroscopy Pads (DEVICE).
Who is sponsoring clinical trial NCT01808183?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01808183 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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