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Outcomes After Laparotomy for Penetrating Abdominal Trauma

Completed
Conditions
Penetrating Abdominal Trauma
Interventions
Procedure: Laparotomy
Registration Number
NCT04536818
Lead Sponsor
Karolinska Institutet
Brief Summary

The purpose of this study is to evaluate outcomes of adult patients hospitalised due to penetrating abdominal trauma at a tertiary trauma hospital in South Africa. Our primary objective is to study the association between waiting time to surgery and outcome (mortality, complications, and length of hospital stay) in normotensive patients treated with laparotomy for penetrating abdominal trauma.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
196
Inclusion Criteria
  • Patients that are admitted due to penetrating abdominal injuries, irrespective of injury mechanism, time from injury and prior treatment.
  • Patients that are treated with laparotomy.
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Exclusion Criteria
  • Patients that are admitted due to blunt trauma or combinations of blunt and penetrating trauma.
  • Patients who are dead on arrival.
  • Patients that are only re-admitted during the study period, i.e. patients that received primary treatment by TBH before study initiation.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Time to surgery ≤12 hoursLaparotomyWaiting time to surgery ≤12 hours from hospital presentation.
Time to surgery >12 hoursLaparotomyWaiting time to surgery \>12 hours from hospital presentation.
Primary Outcome Measures
NameTimeMethod
DeathThrough study completion, an average of 2 weeks

In-hospital death.

Secondary Outcome Measures
NameTimeMethod
ComplicationsThrough study completion, an average of 2 weeks

Complications according to the Clavien-Dindo classification.

Length of stayThrough study completion, an average of 2 weeks

Length of hospital stay.

Trial Locations

Locations (1)

Tygerberg Academic Hospital

🇿🇦

Cape Town, Western Cape Province, South Africa

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