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Bloodstream Infection Due to Multidrug-Resistant Organisms - Multicenter Study on Determinants of Clinical Outcomes (BLOOMY-COM)

U

University Hospital Tuebingen

Status

Unknown

Conditions

Bloodstream Infection
Septic Shock

Study type

Observational

Funder types

Other

Identifiers

NCT03578835
DZIF TTU 08.810

Details and patient eligibility

About

Continual surveillance of both community-acquired and nosocomial bloodstream infections for specific target organisms. Analysis of comorbidities, complications, bacterial resistance patterns, bacterial genomics (e. g. via WGS and MLST typing) for the determinants of clinical outcomes. The clinical outcomes are investigated both in the short-term (up until discharge) and the long-term (six months after index blood culture by standardized questionnaire). A predictive point-of-care score is to be developed based on these data to define high-risk patient populations requiring more intensive diagnostic and/or treatment regimens.

Enrollment

6,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • At least 18 years old
  • Informed consent given either by patient or guardian
  • Inpatient
  • At least one blood culture positive for one of the following bacteria: Staphylococcus aureus, Enterococcus spp., Escherichia coli, Enterobacter spp., Klebsiella spp., Acinetobacter baumannii, Pseudomonas aeruginosa

Exclusion criteria

  • Less than 18 years old
  • Not capable of giving informed consent nor informed consent given by guardian
  • Outpatient
  • No blood cultures positive for any of the target organisms

Trial design

6,000 participants in 1 patient group

Multi-center BSI cohort
Description:
Patients from six German study centers suffering from bloodstream infection caused by specific target organisms.

Trial contacts and locations

6

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Central trial contact

Winfried Kern, Prof.; Evelina Tacconelli, Prof.

Data sourced from clinicaltrials.gov

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