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Clinical Trials/NL-OMON46603
NL-OMON46603
Completed
Not Applicable

Development of a new strategy to predict early sepsis - Sepsis Transcriptome

niversitair Medisch Centrum Groningen0 sites100 target enrollmentTBD
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Conditionssepsisblood infection/poisoning10004018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
sepsis
Sponsor
niversitair Medisch Centrum Groningen
Enrollment
100
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Study subjects (sepsis):
  • •\* Presenting to the Emergency Department (ED)
  • •\* Attending physician suspect sepsis based on at least 2 sign of SIRS criteria and suspicion of infection
  • •\* 19 years of age or greater;Surgical Subjects (control group):
  • •\* Having surgery
  • •\* 19 years of age or greater
  • •\* Subjects already undergoing blood collection during their hospital stay
  • •\* Non\*emergency surgery subjects including ear/nose and throat cases, orthopedic surgery of the major
  • •joints including hip, knee, ankle, shoulder, and wrist.

Exclusion Criteria

  • •\* Patient is terminal (death anticipated in 12 hours)
  • •\* Subjects who are unable to obtain blood as a standard of care.
  • •\* Blood sample could not be taken within 24 hours of a physician first contact in the ED with the patient.

Outcomes

Primary Outcomes

Not specified

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