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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03490305 |
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Date of registration:
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22/03/2018 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Penetrating Abdominal Injuries From the Battle of Mosul
Exlap |
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Scientific title:
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Exploratory Laparotomy Following Penetrating Abdominal Injuries From the Battle of Mosul: a Cohort Study From a Referral Hospital in Erbil, Kurdistan Region in Iraq |
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Date of first enrolment:
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November 11, 2017 |
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Target sample size:
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77 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03490305 |
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Study type:
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Observational [Patient Registry] |
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Study design:
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Phase:
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Countries of recruitment
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Iraq
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Contacts
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Name:
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Johan von Schreeb, MD, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Karolinska Institutet |
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Key inclusion & exclusion criteria
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Inclusion Criteria (all must be fulfilled):
- Penetrating abdominal injury
- Subjected to an exploratory laparotomy at Emergency Hospital, Erbil, Iraq
- Between October 17, 2016 and July 16, 2017
Exclusion Criteria (all must be fulfilled):
- Patients who received treatment several times will only be counted as one patient
- Between October 17, 2016 and July 16, 2017
Age minimum:
N/A
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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War Injury
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Penetrating Abdominal Trauma
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Intervention(s)
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Procedure: Exploratory laparotomy
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Primary Outcome(s)
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Differences in injury mechanism, organs injured, surgical treatment given, postoperative complications and outcome between civilians and combatants.
[Time Frame: an average of 3 weeks]
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Secondary Outcome(s)
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Differences in surgical treatment given, postoperative complications and outcome between patients who receive surgical treatment less than 24 hours from injury and patients who receive surgical treatment more than 24 hours from injury will be analysed.
[Time Frame: an average of 3 weeks]
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Differences in surgical treatment given, postoperative complications and outcome between patients with prior surgical treatment of their injury and patients without prior surgical treatment.
[Time Frame: an average of 3 weeks]
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Secondary ID(s)
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ExlapErbil
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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