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Standardized Perioperative Management of Patients Operated With Acute Abdominal Surgery in a High-risk Emergency Setting

NCT03549624 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1435

Last updated 2022-11-01

No results posted yet for this study

Summary

The objective of the study is to handle patients with the need for an acute laparotomy according to a standardised perioperative protocol and to document the measurement as they are performed (i.e. adherence to the protocol) and to measure the outcome with regard to both short- (30 days) and long-term (3 and 12 months) mortality. Several secondary endpoints will be measured, such as: hospital stay, length of stay at an Intensive Care Unit (ICU), readmission to ICU and surgical complications according to the Clavien-Dindo score. These results will then be compared to published rates of mortality from the literature and to similar outcomes for a cohort of all patients operated at NÄL on the same indication the years prior to the project/study.

Conditions

  • Laparotomy
  • Peritonitis
  • Ileus
  • Perforated Bowel
  • Acute Abdomen

Interventions

OTHER

Standardised protocol for the perioperative management in patients in need of an acute laparotomy

A standardised protocol for the perioperative management of patients including early start of antibiotics and swift surgical intervention as well as an emphasis on repeated monitoring of physiological parameters pre- and post-operatively.

Sponsors & Collaborators

  • NU-Hospital Organization, Sweden

    collaborator OTHER

  • Sahlgrenska University Hospital

    lead OTHER

Principal Investigators

  • Mattias Prytz, MD, PhD · Sahlgrenska University Hospital an NU Hospital Oranization

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-26
Primary Completion
2023-06-01
Completion
2023-09-06

Countries

  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03549624 on ClinicalTrials.gov