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Clinical Trial Summary

Administration of concomitant antibiotics (CA) is a known risk factor for treatment failure in the treatment of CDI, as well as for recurrence of CDI. Recent data suggested that among patients receiving CA, fidaxomicin is superior to vancomycin. While these data are encouraging, many clinicians remain unclear on how to apply these data to patient care. Additionally, patients were excluded from the trials presented to the FDA if it was expected that they would require ≥ 7 days of CA. Therefore, the clinical question still remains of how to apply these data to the real world patient who requires a long course of CA and develops CDI while on therapy. We therefore propose an open label, comparative and prospective study of fidaxomicin 200 mg twice daily vs oral vancomycin 125 mg four times daily for the treatment of CDI among patients who are receiving a long course of CA. We hypothesize that fidaxomicin will be superior to vancomycin with respect to clinical cure for patients with CDI.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02692651
Study type Interventional
Source University of Michigan
Contact
Status Completed
Phase Phase 4
Start date May 1, 2017
Completion date June 23, 2021

See also
  Status Clinical Trial Phase
Recruiting NCT04121169 - Treatment of Mild-moderate Clostridium Difficile Infection (CDI) Phase 2
Completed NCT03244644 - Microbiota Restoration Therapy for Recurrent Clostridium Difficile Infection (PUNCHCD3) Phase 3
Completed NCT02437591 - Study to Evaluate the Pharmacokinetics of Fidaxomicin in Inflammatory Bowel Disease (IBD) Subjects With Clostridium Difficile Infection (CDI) Phase 4
Withdrawn NCT04070352 - Evaluation of Fidaxomicin in the Treatment of Clostridium Difficile Infection (CDI)