- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07582263
MOTORCYCLE THORACIC TRAUMA SEVERITY SCORE: A NEW TRAUMA SEVERITY SCORE (MTTSS)
May 26, 2026 updated by: Antalya Health Sciences University
MOTORCYCLE THORACIC TRAUMA SEVERITY SCORE DEVELOPMENT AND VALIDATION OF A NOVEL PREDICTIVE TOOL FOR MORTALITY AND PULMONARY COMPLICATIONS
This study aimed to test the hypothesis that a practical, bedside-applicable tool could be developed to help identify patients at high risk of mortality following motorcycle accidents more quickly and facilitate treatment by enabling faster clinical decision-making.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Injuries resulting from motorcycle accidents are one of the leading causes of death worldwide, and rates are increasing.
This increase is attributed to the disproportionate vulnerability of riders at the moment of impact, inadequate protective barriers during collisions, motorcycles' ability to reach high speeds and biomechanical exposure.
The thoracic cage is the anatomical region most commonly affected in motorcycle accident-related injuries.
This study aimed to test the hypothesis that a practical, bedside-applicable tool could be developed to help identify patients at high risk of mortality following motorcycle accidents more quickly and facilitate treatment by enabling faster clinical decision-making.
Study Type
Observational
Enrollment (Estimated)
1250
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nilay Cavusoglu Yalcın
- Phone Number: +905057705753
- Email: drnili@hotmail.com
Study Locations
-
-
-
Antalya, Turkey (Türkiye)
- Recruiting
- University of Health Sciences, Antalya Training and Research Hospital
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The study planned to include patients aged 18 years and over who had been involved in a motorcycle accident (as a rider or passenger) and had a chest injury that had been radiologically or clinically confirmed, as well as patients whose medical records had been fully documented during the chart review.
Description
Inclusion Criteria:
- patients aged 18 years or over
- motorcycle accident (a rider or a passenger)
- radiologically or clinically confirmed chest injury
- fully documented in the medical records.
Exclusion Criteria:
- penetrating chest trauma
- patients under the age of 18
- isolated non-chest trauma
- incomplete documentation
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 |
Intervention / Treatment |
|---|---|
|
Training set
|
Training set for model development
|
|
Test set
|
Independent test set for validation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
In-hospital mortality
Time Frame: 30 days after ICU admission
|
30 days after ICU admission
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Develop and validate the model
Time Frame: 30 days after ICU admission
|
30 days after ICU admission
|
|
Assess the model's discriminatory performance, calibration and classification accuracy
Time Frame: 30 days after ICU admission
|
30 days after ICU admission
|
|
Classify patients into clinically meaningful risk categories
Time Frame: 30 days after ICU admission
|
30 days after ICU admission
|
|
Assess the independent contribution of helmet use and chest injury patterns to mortality prediction
Time Frame: 30 days after ICU admission
|
30 days after ICU admission
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Nilay Cavusoglu Yalcın, University of Health Sciences, Antalya Training and Research Hospital
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Lavoie A, Moore L, LeSage N, Liberman M, Sampalis JS. The New Injury Severity Score: a more accurate predictor of in-hospital mortality than the Injury Severity Score. J Trauma. 2004 Jun;56(6):1312-20. doi: 10.1097/01.ta.0000075342.36072.ef.
- Schluter PJ. Trauma and Injury Severity Score (TRISS): is it time for variable re-categorisations and re-characterisations? Injury. 2011 Jan;42(1):83-9. doi: 10.1016/j.injury.2010.08.036.
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 (Actual)
May 6, 2026
Primary Completion (Estimated)
September 6, 2026
Study Completion (Estimated)
October 6, 2026
Study Registration Dates
First Submitted
May 6, 2026
First Submitted That Met QC Criteria
May 6, 2026
First Posted (Actual)
May 12, 2026
Study Record Updates
Last Update Posted (Actual)
May 28, 2026
Last Update Submitted That Met QC Criteria
May 26, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11/10
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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