Evaluation of the Blunt Abdominal Trauma Severity Score (BATSS) in Blunt Abdominal Trauma

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssiut University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Penetrating abdominal trauma

Patients younger than 18 years of age

Pregnant women

Patients referred after definitive surgical intervention at another hospital

Trial population

Adult patients presenting with blunt abdominal trauma to the Emergency Department at Assiut University Hospital within 24 hours of injury.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

120 Participants
are grouped into 1 trial group
Group A: Blunt Abdominal Trauma Patients

Trial outcomes

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.

Time frame
7 days

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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