Overview

Efficacy of Metronidazole Prophylaxis Against Clostridium Difficile-Associated Diarrhea in High Risk Adult Patients

Status:
Terminated
Trial end date:
2016-03-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to test if metronidazole prophylaxis is effective in decreasing the incidence of hospital induced Clostridium Difficile diarrhea among patients at high risk for this infection.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Alison Schneider
Treatments:
Metronidazole
Criteria
Inclusion Criteria:

- Inpatients >55

- Proton Pump inhibitor / Histamine-2 Blocker

- On broad spectrum antibiotics (Zosyn and/or Ciprofloxacin). These two antibiotics are
selected based on current hospital formulary/use

- Anticipated hospital stay >48 hours

- Mental capacity (able to give informed written consent).

Exclusion Criteria:

- Admission for CDI

- Existing diarrhea at admission

- Passed prophylactic window (>48 hours on broad spectrum antibiotics)

- Unable to take PO at the time of evaluation for study entry

- No more than 14 days of broad spectrum antibiotics anticipated

- Medications with serious interactions/contraindications to that would be taken
together with metronidazole (ex. Warfarin, disulfiram, phenytoin, calcineurin
inhibitors)

- Inflammatory Bowel Disease

- Admission for colonic bowel surgery or h/o total/Subtotal colectomy)

- Hospice

- Mortality expected <7days

- Previous CDI in the past 6 months

- Intensive care admission due to the difficulty of monitoring them

- Allergy to Metronidazole or other Antibiotics in protocol

- Patients with neuropathy

- History of heavy ethyl alcohol intake(greater than 3 drinks daily) or intake in past
24 hours,Solid organ transplant.