This study will assess the efficacy of oral vancomycin prophylaxis in preventing recurrent Clostridium difficile infection in hospitalized patients requiring oral or intravenous antibiotics for a suspected or confirmed bacterial infection.
This study will assess the efficacy of oral vancomycin prophylaxis in preventing recurrent Clostridium difficile infection in hospitalized patients requiring oral or intravenous antibiotics for a suspected or confirmed bacterial infection.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
104
Oral vancomycin will be given concurrently with antibiotics to hospitalized patients with a history of Clostridium difficile infection to prevent recurrence
Renown Regional Medical Center
Reno, Nevada, United States
Recurrent Clostridium difficile infection
Diarrheal illness, with at least 3 episodes of watery diarrhea over a 24 hour period and a positive toxin analysis or a positive PCR for Cdiff
Time frame: During hospitalization or the 12 weeks after therapy
Recurrence rate of CDI according to C diff inducing properties of the prescribed antibiotics
* Low inducers: aminoglycosides, fosfomycin, glycopeptides, daptomycin, nitrofurantoin, linezolid, polymyxins, rifamycins, antifolates and/or sulfonamides, tetracyclines, tigecycline * Moderate inducers: penicillins, 1st generation cephalosporins, macrolides, azithromycin, streptogramins * High inducers: carbapenems, 2nd and greater generation cephalosporins, fluoroquinolones, clindamycin
Time frame: During hospitalization or the 12 weeks after therapy
Time between recurrent CDI and the last C diff infection
Time frame: During hospitalization or the 12 weeks after therapy
Rate of recurrence of CDI in immunocompromised patients
HIV, Organ Transplantation, Current Immunosuppressive therapy, Hypogammaglobulinemia or steroids dose more than prednisone 20mg/day for 3 weeks
Time frame: During hospitalization or the 12 weeks after therapy
Rate of recurrence of CDI in patients with a history of the NAP-1 strain
Time frame: During hospitalization or the 12 weeks after therapy
Rate of reported adverse events
Time frame: During hospitalization or the 12 weeks after therapy
Mortality rate
Time frame: During hospitalization or the 12 weeks after therapy
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