drugset / Trial / NCT03030248

Vancomycin for C Difficile NAAT+/EIA- Hematology Oncology Patients

NCT03030248

Phase 2 Completed 9 enrolled Medical College of Wisconsin
RandomizedParallel-groupTriple-blindTreatment

Summary

This study will randomized hematology oncology patients with active diarrhea and a NAAT positive/toxin EIA negative to either 14 days of oral vancomycin capsules or placebo. The study is designed to include 30 patients (15 per arm). Outcomes will include C. difficile load using qPCR, VRE loads, structural and functional microbiome changes and frequency of bowel movements. All endpoints will be measured at several time points including days 0, 14, 21 and 90.

Timeline

Start
2018-06-01
Primary completion
2020-06-30
Completion
2020-06-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Vancomycin Other / unclassified 125 mg Oral