Efficacy of Metronidazole Prophylaxis Against Clostridium Difficile-Associated Diarrhea in High Risk Adult Patients
Primary Purpose
Clostridium Difficile Diarrhea
Status
Terminated
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Metronidazole
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Clostridium Difficile Diarrhea focused on measuring Clostridium difficile infection, Diarrhea, Flagyl, Metronidazole
Eligibility 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.
Sites / Locations
- Cleveland Clinic Florida
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Metronidazole
Placebo
Arm Description
Metronidazole tablets 500mg orally or IV , 3 times a day for a maximum of 14 days
Placebo(Corn starch pill) orally 3 times a day for a maximum of 14 days
Outcomes
Primary Outcome Measures
The Incidence of Clostridium Difficile Diarrhea in Both Study Groups at 30 Days Post Broad Spectrum Antibiotic Use.
Secondary Outcome Measures
Determine Differences in Clostridium Difficile Diarrhea Incidence Between Patients on Piperacillin/Tazobactam vs. Patients on Ciprofloxacin.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02200328
Brief Title
Efficacy of Metronidazole Prophylaxis Against Clostridium Difficile-Associated Diarrhea in High Risk Adult Patients
Official Title
Efficacy of Metronidazole Prophylaxis Against Clostridium Difficile-Associated Diarrhea in High Risk Adult Patients: A Randomized Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Terminated
Why Stopped
Patients noncompliant with instructions and follow ups could not be completed.
Study Start Date
August 2014 (undefined)
Primary Completion Date
March 2016 (Actual)
Study Completion Date
March 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Alison Schneider
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief 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.
Detailed Description
Clostridium Difficile infection or C. Diff (CDI) is an infection that causes severe diarrhea. Risk factors for this infection include hospitalization, the use of antibiotics, along with medications that decrease the acid in the stomach. This infection leads to a disease which is difficult to treat and can cause serious complications including death in rare cases. This infection also increases medical costs by prolonging hospital stays.
Metronidazole (known by the brand name Flagyl) is an antibiotic that has been available for decades and has been used to treat this disease. Flagyl is approved by the Food and Drug Administration for the treatment of C. diff infection. Recent research by the investigators group has shown that hospitalized patients who took Flagyl had a decreased chance of getting C. Diff infection. However, high quality studies are needed to better evaluate whether the investigators can prevent C. Diff infection in high risk patients with the use of Flagyl.
The purpose of this study is to assess if metronidazole prophylaxis is effective in decreasing the incidence of hospital induced Clostridium Difficile diarrhea among inpatients at high risk for this infection.
High risk patient population are as defined below: taking a broad spectrum antibiotics (piperacillin/tazobactam-Zosyn; Ciprofloxacin).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clostridium Difficile Diarrhea
Keywords
Clostridium difficile infection, Diarrhea, Flagyl, Metronidazole
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
76 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Metronidazole
Arm Type
Experimental
Arm Description
Metronidazole tablets 500mg orally or IV , 3 times a day for a maximum of 14 days
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo(Corn starch pill) orally 3 times a day for a maximum of 14 days
Intervention Type
Drug
Intervention Name(s)
Metronidazole
Other Intervention Name(s)
Flagyl
Intervention Description
Metronidazole tablets 500mg orally or IV , 3 times a day for a maximum of 14 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
corn starch pill
Intervention Description
Placebo(Corn starch pill) orally 3 times a day for a maximum of 14 days
Primary Outcome Measure Information:
Title
The Incidence of Clostridium Difficile Diarrhea in Both Study Groups at 30 Days Post Broad Spectrum Antibiotic Use.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Determine Differences in Clostridium Difficile Diarrhea Incidence Between Patients on Piperacillin/Tazobactam vs. Patients on Ciprofloxacin.
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility 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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alison Schneider, M.D.
Organizational Affiliation
Cleveland Clinic Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic Florida
City
Weston
State/Province
Florida
ZIP/Postal Code
33331
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Efficacy of Metronidazole Prophylaxis Against Clostridium Difficile-Associated Diarrhea in High Risk Adult Patients
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