- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07803211
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
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.
Study Overview
Status
Study Type
Enrollment (Estimated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participants Requiring Operative Management
Time Frame: 7 days
|
Number of participants with blunt abdominal trauma who undergo surgical operative intervention (such as exploratory laparotomy) during hospitalization.
|
7 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
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
- BATSS in Blunt Abdomen Trauma
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.