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.
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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

Meghan A Baker, MD, SCD

617-732-8881

mbaker1@bwh.harvard.edu

CONTACT

Sanjat Kanjilal, MD, MPH

skanjilal@bwh.harvar.edu

CONTACT