Primary Prophylaxis of Clostridioides Difficile Infection With Oral Vancomycin

Withdrawn before enrolling · Phase 2/Phase 3

Conditions studied: Clostridioides Difficile, Vancomycin Resistance Enterococcus Faecium

In brief

The purpose of this study is to evaluate the ability of oral vancomycin in preventing Clostridioides difficile infection (CDI) in patients that are simultaneously receiving antibiotics. Participants in this study will be placed randomly into two groups. The oral vancomycin treatment group will receive oral vancomycin two times per day simultaneously with an antibiotic plus two additional days. The no oral vancomycin control group will receive the current standard of care, which is an antibiotic and no oral vancomycin. Participation in this study will last approximately 3 months.

Key facts

Study ID
NCT07221708
Run by
University of Maryland, Baltimore
People needed
0
Starts
2027-01-01
Expected to finish
2027-12-31
Last updated by the study team
2026-07-29

Who can join

Age: 65 and older, up to 100. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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