Evaluation of the Blunt Abdominal Trauma Severity Score (BATSS) in Blunt Abdominal Trauma
Prospective Evaluation of the Blunt Abdominal Trauma Severity Score (BATSS) for Predicting Clinical Outcomes in Patients With Blunt Abdominal Trauma at Assiut University Hospitals
1 other identifier
observational
120
0 countries
N/A
Brief Summary
Blunt abdominal trauma (BAT) is a leading cause of trauma-related morbidity and mortality, commonly caused by motor vehicle collisions, falls, and assaults. Early identification of significant intra-abdominal injury remains a major diagnostic challenge because physical examination alone has limited sensitivity in patients with altered consciousness or distracting injuries. The Blunt Abdominal Trauma Severity Score (BATSS) is a rapid bedside assessment tool that integrates clinical signs, hemodynamic parameters, and Focused Assessment with Sonography for Trauma (FAST) findings to risk-stratify patients presenting with blunt abdominal trauma. This prospective observational cohort study aims to evaluate the diagnostic accuracy and clinical utility of BATSS in adult patients presenting with blunt abdominal trauma to the Emergency Department at Assiut University Hospitals. Enrolled participants will be scored upon initial presentation and categorized into low-, moderate-, or high-risk groups to assess the score's ability to predict the definitive mode of management (operative intervention versus conservative observation), intensive care unit (ICU) admission, in-hospital mortality, and post-traumatic complications.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Oct 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 31, 2026
CompletedFirst Posted
Study publicly available on registry
September 3, 2026
CompletedStudy Start
First participant enrolled
October 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
November 1, 2027
September 3, 2026
August 1, 2026
1 year
August 31, 2026
August 31, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of Participants Requiring Operative Management
Number of participants with blunt abdominal trauma who undergo surgical operative intervention (such as exploratory laparotomy) during hospitalization.
7 days
Study Arms (1)
Blunt Abdominal Trauma Patients
Adult patients aged 18 years or older presenting with blunt abdominal trauma to the Emergency Department within 24 hours of injury. All enrolled patients undergo initial trauma assessment according to the ATLS protocol, including a Focused Assessment with Sonography for Trauma (FAST) examination. The Blunt Abdominal Trauma Severity Score (BATSS) is calculated upon admission to stratify patients into low-risk (\<8 points), moderate-risk (8-11 points), and high-risk (≥12 points) groups. Subsequent diagnostic evaluations (such as contrast-enhanced CT) and management pathways (operative intervention vs. conservative observation) are recorded and followed up to assess outcomes.
Eligibility Criteria
Adult patients presenting with blunt abdominal trauma to the Emergency Department at Assiut University Hospital within 24 hours of injury.
You may qualify if:
- Patients aged 18 years or older
- Patients presenting with blunt abdominal trauma
- Patients presenting within 24 hours of injury
- Patients who undergo initial trauma assessment including Focused Assessment with Sonography for Trauma (FAST) examination
- Patients (or their legal guardians) who provide written informed consent
You may not qualify if:
- Penetrating abdominal trauma
- Patients younger than 18 years of age
- Pregnant women
- Patients referred after definitive surgical intervention at another hospital
- Patients with incomplete clinical or radiological data
- Patients who refuse participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Resident at Emergency Department
Study Record Dates
First Submitted
August 31, 2026
First Posted
September 3, 2026
Study Start
October 1, 2026
Primary Completion (Estimated)
October 1, 2027
Study Completion (Estimated)
November 1, 2027
Last Updated
September 3, 2026
Record last verified: 2026-08