Pre-emptive Prevention for Patients at High Risk for Hospital-onset Clostridioides Difficile
Recruiting
N/A
Interventional Study
C. Difficile
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 300 (estimated)
- Sponsor
- Brigham and Women's Hospital · Other
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About This Trial
Clostridioides difficile (C. difficile) is the most common healthcare-associated pathogen, causing \>500,000 infections and \>29,000 deaths per year in the US. Traditional approaches to reduce hospital-onset CDI focus on identifying, isolating, and treating symptomatic patients to prevent transmission to other patients. Recent genomic epidemiology studies, however, suggest that most hospital-onset…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients admitted to ICU or Oncology units and identified to carry C. Difficile via VRE swab
Exclusion Criteria:
* Patients not identified as carriers of C. difficile and patients not admitted to ICU or oncology units
Contacts