- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01540318
Utility of Abdominal Ultrasound in the Evaluation of Children With Blunt Trauma
The major goal of this project is to conduct a randomized controlled trial studying an initial evaluation strategy with abdominal ultrasound versus a strategy without abdominal ultrasound for the evaluation of children with blunt abdominal trauma. The proposal's objectives are to compare the following variables in those that randomize to abdominal ultrasound versus those that do not:
- rate of abdominal CT scanning
- time to emergency department disposition
- the rate of missed/delayed diagnosis of intra-abdominal injury
- the costs.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
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Sacramento, California, United States, 95817
- UC Davis Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Blunt torso trauma resulting from a significant mechanism of injury
- Motor vehicle collision: greater than 60 mph, ejection, or rollover
- Automobile versus pedestrian/bicycle: automobile speed > 25 mph
- Falls greater than 20 feet in height
- Crush injury to the torso
- Physical assault involving the abdomen
- Decreased level of consciousness (Glasgow Coma Scale score < 15 or below age-appropriate behavior) in association with blunt torso trauma
Blunt traumatic event with any of the following (regardless of the mechanism):
- Extremity paralysis
- Multiple long bone fractures (e.g., tibia and humerus fracture)
- History and physical examination suggestive of intra-abdominal injury following blunt torso trauma of any mechanism (including mechanisms of injury of less severity than mentioned above)
Exclusion Criteria:
- No concern for inter-abdominal injury or no planned evaluation for possible IAI
- Prehospital or ED age adjusted Hypotension
- Prehospital or initial ED GCS score ≤ 8
- Presence of an abdominal "seat belt sign" - continuous area of erythema/contusion completely across the lower abdomen secondary to a lap belt
- Penetrating trauma: stab or gunshot wounds
- Traumatic injury occurring > 24 hours prior to the time of presentation to the ED
- Transfer of the patient to the UCDMC ED from an outside facility with abdominal CT scan, diagnostic peritoneal lavage, or laparotomy previously performed
- Patients with known disease processes resulting in intraperitoneal fluid including liver failure and the presence of ventriculoperitoneal shunts
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Abdominal Ultrasound
Patients in the experimental arm will receive a "Focused Assessment with Sonography for Trauma (FAST)" which includes the use of abdominal ultrasound.
|
Use of FAST abdominal ultrasound exam
Other Names:
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No Intervention: No Abdominal Ultrasound
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Rate of Abdominal CT Scan
Time Frame: One week from enrollment
|
One week from enrollment
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Total time spent in the Emergency Department
Time Frame: 24 hours from enrollment
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24 hours from enrollment
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Cost effectiveness
Time Frame: two months from enrollment
|
two months from enrollment
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: James F Holmes, MD, MPH, UC Davis School of Medicine
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 244545 (Other Identifier: UC Davis)
- H34MC19682 (Other Grant/Funding Number: US Department of Health and Human Services)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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