- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06737874
Predictive Value of Revised Trauma Score(RTS)and Glasgow Coma Scale (GCS)of Mortality in Patients with Multiple Trauma.
December 12, 2024 updated by: Abd Elrhman Salah Abuozied Mansour, Assiut University
Predictive Value of Revised Trauma Score(RTS)and Glasgow Coma Scale (GCS)of Mortality in Patients with Multiple Trauma in Emergency Department At Assiut University Hospital & Ismailia University Hospitals.
This study aims to assess the efficacy of RTS and GCS in predicating the mortality among multiple trauma patients admitted to emergency departments at Assiut university hospital.Which score is better in predicting mortality in polytrauma patients Revised Trauma Score (RTS) or Glasgow Coma Scale (GCS) of with Multiple Trauma?
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
Trauma is a serious global health problem.
Globally around 5.8 million people deaths were estimated from injuries in 2004.
These deaths accounted for 10% of the world's mortality[1].
It is the fifth leading cause ofsignificant, disability and sixth leading cause of death[2].
More than 90% of the world's injury deaths occur in low- and middle-income countries[3].
Injury deaths in Egypt accounted for 8% and the eighth leading cause of death in 2010[4].
There was an increase in the number of hospitalization due to trauma.
In Upper Egypt, trauma cases increased from 19,869 up to 32,699 with death rate 1.2/100 cases per year throughout the period from 2002 to 2009.In multiple trauma patient management, time is crucial.
Early intervention has consistently been shown to reduce mortality and morbidity[5].
Prompt and effective care [6].
These scores either measure the alteration in patient's physiology; Glasgow Coma Scale (GCS) and Revised Trauma Score (RTS) or anatomy; Injury Severity Score (ISS)[7].
Glasgow Coma Scale (GCS) is one of the most commonly used trauma scores and is a good predictor of the outcome.
The GCS is primarily utilized to evaluate the level of consciousness impairment in patients, achieved through the assessment of ocular, motor, and verbal response[8].The Revised Trauma Score (RTS) are considered the most practical and effective [9].The RTS stands out because it can be quickly calculated using a patient's initial clinical status and vital signs at presentation, making it particularly useful during the critical "golden hour" after arrival[10]
Study Type
Observational
Enrollment (Estimated)
100
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: Abd Elrahman Salah Mansour, Resident doctor
- Phone Number: +201153019392
- Email: salaaabdo13@gmail.com
Study Contact Backup
- Name: Bassant Sayed Abdallah, Lecturer of Emergency medicine
- Phone Number: +201227062927
- Email: Bassant_Sayed@med.suez.edu.eg
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
multiple trauma patients admitted to Emergency department.
The Berlin definition defines polytrauma as a life-threatening injury involving at least 2 bodily regions (each with an AIS ≥3) as well as at least one positive physiologic parameter.
The physiologic parameters include the elderly (age ≥70 years), low systolic blood pressure, Glasgow coma score ≤8, coagulopathy, and acidosis[17].
Description
Inclusion Criteria:
- 1-patients aged from > 18 years old. 2-Both male and female. 3-Patients have penetrating and blunt trauma.
Exclusion Criteria:
- 1-Pregnant women. 2-Patients with mild trauma such as soft tissue damage and 3-isolated limb fractures. 4-Patients were transferred to another hospital. 5-Failure of follow-up for any reason. 6-Patients who refused participatioc.
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 |
|---|
|
group A
polytrauma patients
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
mortality rate
Time Frame: 30 day
|
to identify the trauma-related mortality rate among patients
|
30 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Admission
Time Frame: 30days
|
Associated risk factors that affect multiple trauma patient's outcome.
Outcome of patients :(death/survival) with 30 day of admission , hospital stay, and ICU admission
|
30days
|
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 (Estimated)
January 10, 2025
Primary Completion (Estimated)
December 30, 2025
Study Completion (Estimated)
December 1, 2026
Study Registration Dates
First Submitted
December 2, 2024
First Submitted That Met QC Criteria
December 12, 2024
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
December 12, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RTS & GCS in trauma patients
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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