Pre-emptive Prevention for Patients at High Risk for Hospital-onset Clostridioides Difficile
Eligible age
18+ yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
See if you qualify for this study
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About this study
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 CDI cases are attributable to asymptomatic carriers who either progress from colonization to active infection themselves or transmit C. difficile to other patients while asymptomatic. This trial will evaluate an intervention to pre-emptively identify asymptomatic C. difficile carriers and then implement a patient-tailored prevention package to protect the carrier from progression to active infection and to prevent transmission from the carrier to other patients.
Sponsor: Brigham and Women's Hospital
You may qualify if…
- ✓ Patients admitted to ICU or Oncology units and identified to carry C. Difficile via VRE swab
You may not qualify if…
- ✕ Patients not identified as carriers of C. difficile and patients not admitted to ICU or oncology units
Where it's recruiting
Boston
Source: ClinicalTrials.gov · NCT05389904 · last updated 2026-03-04