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Hematological Infection Score Compared to the Hospital Standard for Diagnosis of SIRS or Sepsis on ICU

Charité University Medicine Berlin logo

Charité University Medicine Berlin

Status

Completed

Conditions

SIRS
Sepsis

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01236703
HemoSIRS

Details and patient eligibility

About

CRP and PCT are not valid parameters of early infection in particularly postoperative patients. (Sanders et al., A&A, June 2006, Vol.102; Katja et al., Shock, February 2001, Vol 15.2) Better detection systems for SIRS and sepsis are urgently required.

ICIS® (Sysmex intensive care infection score) and ICPS® (Sysmex intensive care prognostic score) are two new score-systems depending on detectable cellular response of the innate immune system in human peripheral blood.

The purpose of this observational study is to determine if these scores are superior in early differentiation between non-infectious SIRS and infectious SIRS (sepsis) in postoperative patients. Furthermore, the applicability of the scores for triggering start and ending of anti-infective therapy will be examined.

Enrollment

207 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • all ICU patients age > 18 years
  • more than 36h on ICU

Exclusion criteria

  • ICU patients age < 18 years
  • less than 36h on ICU

Trial design

207 participants in 1 patient group

ICU patients
Description:
ICU patients (post-operative and none operative patients) will be enrolled in the study. They are followed up until the end of ICU stay or, for a maximum of 60 days.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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