Development of a new strategy to predict early sepsis
- Conditions
- blood infection/poisoning10004018sepsis
- Registration Number
- NL-OMON46603
- Lead Sponsor
- niversitair Medisch Centrum Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
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.
* 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.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method