Compassionate Use of Nitazoxanide for the Treatment of Clostridium Difficile Infection
Clostridium Enterocolitis, Pseudomembranous Colitis
About this trial
This is an interventional treatment trial for Clostridium Enterocolitis focused on measuring Clostridium difficile Associated Diarrhea
Eligibility Criteria
Inclusion Criteria: Patient must be > 18 years of age Clinical diagnosis of C. difficile associated disease, based on the new onset of diarrhea, abdominal discomfort, or otherwise unexplained fever or leukocytosis Diagnosis of C. difficile colitis proven by positive assay for C. difficile toxin in feces Disease has been treated, and the symptoms failed to respond to treatment with metronidazole or vancomycin, or symptoms promptly relapsed after completing a course of therapy with either of these drugs Able to take oral medication Exclusion Criteria: Patients with other recognized causes of diarrhea or colitis Women of child bearing age who are pregnant, breast feeding, or not using birth control Patients taking coumadin, phenytoin, celecoxib, or losartan Patients with renal insufficiency (BUN or creatinine >2 times baseline) Serious systemic disorder incompatible with the study
Sites / Locations
- Baylor College of Medicine
- Michael E. Debakey VA Medical Center
Arms of the Study
Arm 1
Other
active drug
500 mg nitazoxanide bid given to patient