Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • C. Diff Colitis
  • C.Difficile Colitis
  • C.Difficile Diarrhea
  • CDI
  • Clostridium Difficile Infection
  • Recurrent Clostridium Difficile Infection
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Participant, Investigator)Primary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Many patients who have a CDI experience recurrent or relapsing symptoms. The investigators are studying whether vancomycin in low doses will help prevent further CDI episodes and how this therapy impacts patients' gastrointestinal microbiome and composition. Patients with a history of past CDI who a...

Many patients who have a CDI experience recurrent or relapsing symptoms. The investigators are studying whether vancomycin in low doses will help prevent further CDI episodes and how this therapy impacts patients' gastrointestinal microbiome and composition. Patients with a history of past CDI who are receiving antibiotics for a non-CDI condition will be invited to participate. Approximately half of the participants will receive a low-dose capsule of vancomycin and half will receive a placebo. Participants will continue taking the vancomycin/placebo for 5 days after their prescribed antibiotics end.

Tracking Information

NCT #
NCT03462459
Collaborators
  • Medical College of Wisconsin
  • Agency for Healthcare Research and Quality (AHRQ)
  • Henry Ford Hospital
Investigators
Principal Investigator: Nasia Safdar, MD PhD University of Wisconsin, Madison