- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03686579
Chest Trauma :Prediction of Thoracic Injuries Clinically and Radiologically (chesttrauma)
April 14, 2019 updated by: alzahraa gamal hasanein, Assiut University
Chest Trauma:Prediction of Associated Thoracic Injuries by Clinical and Radiological Studies .Specificity and Sensitivity
• Trauma is a major cause of morbidity and mortality worldwide.
Despite the advent of specialized trauma centers the outcome of patients who sustain major trauma remains disappointing.
Plain radiography and more advanced imaging techniques such as ultrasound, computerised tomography (CT) and angiography, have a major role to play in the early decision making and subsequent management of patients who sustain polytrauma.
This article discusses the choice of emergency imaging techniques available in chest trauma for clinicians and radiologists; their evaluation and some of the common pitfalls that may lead to errors of interpretation.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Imaging plays a key role for both, the primary diagnostic work-up, and the secondary assessment of potential treatment.
Despite its well-known limitations, the posteroanterior chest radiograph remains the starting point of the imaging work-up.
Adjunctive imaging with computed tomography, that recently is increasingly often performed on multidetector computed tomography units, adds essential information not readily available on the conventional radiograph.
This allows better definition of trauma-associated thoracic injuries not only in acute traumatic aortic injury, but also in pulmonary, tracheobronchial, cardiac, diaphragmal, and thoracic skeletal injuries.
This article reviews common radiographic findings in patients after chest trauma, shows typical imaging features resulting from thoracic injury, presents imaging algorithms, and recalls to the reader less common but clinically relevant entities encountered in patients after thoracic trauma.
Study Type
Observational
Enrollment (Anticipated)
70
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Information collected by this study may contribute to the care of patients in the future who have the same lesions as those that participate in this study.
The information may also improve the future management of study participants.
On the other hand patients will benefit from the clinical and radiological follow up postoperatively.
There are no known risks associated with participation in this study.
Patients' treatment and follow up will not be altered by any means
Description
Inclusion Criteria:
- chest trauma 2. recent trauma: presented within48 h
Exclusion Criteria:
- Old trauma more than 48h 2-Pt transferred urgently to operating room
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
- Observational Models: Cohort
- Time Perspectives: Other
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
chest trauma
|
clinical and radiological study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
detection of associated thoracic injuries : fracture rib ,sternum…. etc detection of sensitivity and specificity of clinical and radiological finding detection of associated thoracic injuries : fracture rib ,sternum…. etc
Time Frame: after one week
|
prediction of associated thoracic injuries by clinical and radiological studies .specificity
and sensitivity
|
after one week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Alzahraa gamal hasanien sayed, Assiut University
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 (Anticipated)
November 1, 2019
Primary Completion (Anticipated)
November 1, 2020
Study Completion (Anticipated)
December 1, 2020
Study Registration Dates
First Submitted
September 25, 2018
First Submitted That Met QC Criteria
September 26, 2018
First Posted (Actual)
September 27, 2018
Study Record Updates
Last Update Posted (Actual)
April 16, 2019
Last Update Submitted That Met QC Criteria
April 14, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CT
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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