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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03618446
Other study ID # 17100526
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2010
Est. completion date September 2017

Study information

Verified date February 2022
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A retrospective cohort study was carried out for all pelvic fracture patients admitted to Assiut University Trauma Unit (AUTU), a level-1 trauma center. (AUTU) is located in Upper Egypt and provides healthcare to over 30,000 patients per year.


Description:

In 2010, a Pelvic Injury Registry was developed to document treatment and outcomes in a standardized manner. All patients admitted to AUTU sign an informed consent to permit using their data for research purposes. Patients' data are prospectively collected and stored in a local database specifically designed for this purpose. Data collected included age, gender, mechanism of injury, fracture classification, associated injuries, and admission to ICU, the length of hospital stay and presence of abdominopelvic collection as diagnosed by Focused Assessment with Sonography for Trauma (FAST) at admission. The primary outcome measure was in-hospital mortality. Predictors of in-hospital mortality were identified by comparing characters of survivors and non-survivors. Secondary objectives were to analyse the differences between adults and children and to analyse the causes and timing of death.


Recruitment information / eligibility

Status Completed
Enrollment 1188
Est. completion date September 2017
Est. primary completion date December 31, 2013
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - first-time admissions and patients whose treatment was completed at our hospital - all pelvic fracture patients admitted to our Trauma Unit. Exclusion Criteria: - penetrating injuries - isolated acetabular fractures - Patients who were discharged on their own will against the medical advice or whose treatment was continued at another hospital - re-admitted patients - Firearm injuries

Study Design


Related Conditions & MeSH terms


Intervention

Other:
The presence of a pelvic fracture


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Assiut University AO Clinical Investigation and Publishing Documentation

Outcome

Type Measure Description Time frame Safety issue
Primary in-hospital mortality Death occurring while the patient is admitted in the hospital. One month
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