- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05538390
Assessment of Pattern of Abdominal Injury
September 10, 2022 updated by: St. Paul's Hospital Millennium Medical College, Ethiopia
Assesment of Pattern of Abdominal Injury Over a Two Year Period at St Paul's Hospital Millennium Medical College and AaBET Hospital, Addis Ababa, Ethiopia: A Retrospective Study
This hospital-based cross-sectional study was done at SPHMMC and AaBET hospitals from January 2018 to December 2019.The study aimed to assess the pattern of abdominal injury at St Paul's Hospital Millennium Medical College (SPHMMC) and Addis Ababa Burn, Emergency and Trauma (AaBET) hospital, Addis Ababa Ethiopia.Data was collected from the trauma registry and patient files using a pretested structured questionnaire filled out by two trained data collectors.The collected data was entered and analyzed using statistical software SPSS version 25.0.
Study Overview
Detailed Description
Data was collected from the trauma registry and patient files using a pretested structured questionnaire filled out by two trained data collectors.
The questionnaire was categorized into socio-demographics (age, sex, residency, and address), clinical profile (triage, v/s, type of injury, associated injury), management, and outcome (management, complication, disposition, and mortality).
Completeness of data was checked by the principal investigator.
Study Type
Observational
Enrollment (Actual)
165
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Addis Ababa, Ethiopia, 1000
- St Paul's Hospital Millennium Medical College
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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
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
all patients who presented to the AaBET and SPHMMC Hospital emergency department with a clinical diagnosis of abdominal trauma during the study period.
Description
Inclusion Criteria:
- All patients who are diagnosed clinically to have abdominal trauma
Exclusion Criteria:
- Patients who died before diagnosis
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pattern of Abdominal Injury
Time Frame: Over 2 years
|
Frequency was analyzed in respective to socio-demographics (age, sex, residency, address), clinical profile(triage, v/s, type of injury, associated injury), management and outcome (management, complication, disposition and mortality) in patients presented with Abdominal injury in the study period.
|
Over 2 years
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Kassaye D Altaye, University of Gondar
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Alastair, C.J., Pierre, J.G. Abdominal trauma. In: John M, Graeme D, Kevin OM, editors. Surgical Emergencies, 1st edition. Italy: Blackwell Science Ltd. 1999. 224-236
- Adesanya AA, Afolabi IR, da Rocha-Afodu JT. Civilian abdominal gunshot wounds in Lagos. J R Coll Surg Edinb. 1998 Aug;43(4):230-4.
- Long MK, Vohra MK, Bonnette A, Parra PDV, Miller SK, Ayub E, Wang HE, Cardenas-Turanzas M, Gordon R, Ugalde IT, Allukian M, Smith HE. Focused assessment with sonography for trauma in predicting early surgical intervention in hemodynamically unstable children with blunt abdominal trauma. J Am Coll Emerg Physicians Open. 2022 Jan 27;3(1):e12650. doi: 10.1002/emp2.12650. eCollection 2022 Feb.
- Abebe K, Bekele M, Tsehaye A, Lemmu B, Abebe E. Laparotomy for Abdominal Injury Indication & Outcome of patients at a Teaching Hospital in Addis Ababa, Ethiopia. Ethiop J Health Sci. 2019 Jul;29(4):503-512. doi: 10.4314/ejhs.v29i4.12.
- Chalya PL, Mabula JB. Abdominal trauma experience over a two-year period at a tertiary hospital in north-western Tanzania: a prospective review of 396 cases. Tanzan J Health Res. 2013 Oct;15(4):230-9.
- AdejumoAA,ThairuY,EgentiN.Profile of abdominal trauma in federal teaching hospital, Gombe, North-east, Nigeria: A cross sectional study. Int J Innov Med Health Sci 2015; 4: 41-5
- Bashah DT, Dachew BA, Tiruneh BT. Prevalence of injury and associated factors among patients visiting the Emergency Departments of Amhara Regional State Referral Hospitals, Ethiopia: a cross-sectional study. BMC Emerg Med. 2015 Aug 25;15:20. doi: 10.1186/s12873-015-0044-3.
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 (ACTUAL)
September 1, 2019
Primary Completion (ACTUAL)
May 30, 2020
Study Completion (ACTUAL)
June 10, 2020
Study Registration Dates
First Submitted
September 5, 2022
First Submitted That Met QC Criteria
September 10, 2022
First Posted (ACTUAL)
September 13, 2022
Study Record Updates
Last Update Posted (ACTUAL)
September 13, 2022
Last Update Submitted That Met QC Criteria
September 10, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- StPaulsHMMc
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The data used to support the findings of this study are available from the Principal investigator upon request.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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