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Outcomes After Laparotomy for Penetrating Abdominal Trauma

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Karolinska Institute

Status

Completed

Conditions

Penetrating Abdominal Trauma

Treatments

Procedure: Laparotomy

Study type

Observational

Funder types

Other

Identifiers

NCT04536818
TraumaLapCohort

Details and patient eligibility

About

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.

Enrollment

196 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

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.

Trial design

196 participants in 2 patient groups

Time to surgery ≤12 hours
Description:
Waiting time to surgery ≤12 hours from hospital presentation.
Treatment:
Procedure: Laparotomy
Time to surgery >12 hours
Description:
Waiting time to surgery \>12 hours from hospital presentation.
Treatment:
Procedure: Laparotomy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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