- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02011412
Intermountain Risk Score and Trauma
February 22, 2016 updated by: Sarah Majercik, Intermountain Health Care, Inc.
The Intermountain Risk Score's Association With Mortality Prediction in Trauma Patients
The investigators hypothesize that a risk score composed of age, sex, and the components of commonly ordered laboratory panels will be predictive of mortality in trauma patients, and will help improve clinicians' ability to make more accurate mortality predictions at the time of admission.
Study Overview
Study Type
Observational
Enrollment (Actual)
400
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Utah
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Murray, Utah, United States, 84107
- Intermountain Medical Center
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Individuals who suffer from a traumatic injury and present to the Emergency Department as a Trauma Activation
Description
Inclusion Criteria:
- Patient presents to Intermountain Medical Center as a Level I or Level II trauma activation.
- Age ≥18
Exclusion Criteria:
Patients who are not admitted to the hospital
- Patients who expire in the Emergency Department
- Patients who are discharged to home from the Emergency Department
- Patients who do not have a complete blood count and basic metabolic profile drawn in the Emergency Department as part of routine clinical care.
- Patients who enter the hospital as "trauma consults." These patients have traumatic injuries, and are often admitted to the trauma service, but the severity of their trauma is not thought to warrant trauma team activation.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Intermountain Risk Score known
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Intermountain Risk Score Unknown
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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all cause mortality
Time Frame: 30 days
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To determine whether the Intermountain Risk Score accurately predicts 30 day mortality and one year mortality in trauma patients.
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30 days
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all cause mortality
Time Frame: 1 year
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measure the ability of the Intermountain Risk Score to predict all cause mortality at one year after the traumatic event
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1 year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
experienced clinicians mortality prediction
Time Frame: 30 days
|
compare the IMRS to experienced clinicians' ability to predict mortality at 30 days
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30 days
|
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Experienced Clinicians' mortality prediction
Time Frame: 1 year
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compare the IMRS to experienced clinicians' ability to predict mortality at 1 year
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1 year
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2013
Primary Completion (Actual)
December 1, 2015
Study Completion (Actual)
December 1, 2015
Study Registration Dates
First Submitted
November 6, 2013
First Submitted That Met QC Criteria
December 10, 2013
First Posted (Estimate)
December 13, 2013
Study Record Updates
Last Update Posted (Estimate)
February 24, 2016
Last Update Submitted That Met QC Criteria
February 22, 2016
Last Verified
February 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1024710
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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