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Diagnostic of Infections Following Major Abdominal Surgery and Burn Injury

Impact of Biomarkers for Early Diagnostic of Infections Following Major Abdominal Surgery and Severe Burn Injuries

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01055587
Acronym
Earlygnost
Enrollment
120
Registered
2010-01-25
Start date
2009-09-30
Completion date
2015-06-30
Last updated
2017-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Second Degree Burn, Third Degree Burn

Keywords

major abdominal surgery, severe burn injury, infection, diagnostic

Brief summary

This study was designed to investigate, if new biomarkers may improve the early diagnostic of infections following major abdominal surgery and severe burn injuries.

Interventions

None listed

Sponsors

Martin-Luther-Universität Halle-Wittenberg
CollaboratorOTHER
Klinikum St. Georg gGmbH
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients with major abdominal surgery (e.g. gastrectomy, hemi-/colectomy, resection of sigma or rectum, resection of liver, esophagectomy) * patients following severe burn injury (burn surface area \>= 15%) * age \>= 18 years * informed consent

Exclusion criteria

* no informed consent * emergency surgery * immunocompromising diseases (e.g. HIV+, AIDS, Lymphoma or NonHodgkin-Lymphoma, Autoimmune-Diseases) * pre-existing liver or renal failure * chronic therapy with corticoids

Design outcomes

Primary

MeasureTime frame
rate of infectionsday 28 post intervention

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026