Clostridium Difficile Clinical Trial
Official title:
Fecal Microbiota Transplantation for Relapsing Clostridium Difficile Infection
There has been an alarming increase in the incidence and severity of Clostridium difficile infection (CDI) in North America over the past decade. Relapsing infection is a common problem in patients treated for CDI, often requiring prolonged and expensive courses of oral vancomycin with limited alternative treatment options. This study will determine if fecal microbiota transplantation, which involves administering fecal flora from a healthy stool donor to a patient with relapsing CDI, is an effective and safe treatment.
Clostridium difficile is an increasingly common infection. The number of hospital discharges
for which C. difficile was listed as the first diagnosis more than doubled between 2000 and
2003. In addition to occurring more frequently, there is an epidemic of serious cases which
are more refractory to therapy and which have high rates of colectomy and death. Most
commonly, C. difficile infection (CDI) is associated with use of antimicrobial agents that
are thought to alter the normal bacterial flora of the gastrointestinal tract so as to
permit colonization and/or proliferation and toxin elaboration by C. difficile. Though the
precise mechanisms by which this occurs are still incompletely understood, depletion of
physiologic microflora, in particular Bacteroides species may play an important role. Most
patients with CDI respond to a course of oral metronidazole or vancomycin, however, up to
20% of patients relapse after initial treatment. Current guidelines recommend a tapering
course of vancomycin after a second recurrence, however up to 60% of patients still do not
respond to this treatment strategy or develop further recurrence after the vancomycin is
stopped. Use of antimicrobials to treat CDI may predispose these patients to further
relapses through the maintenance of disturbed intestinal flora and may contribute to the
emerging problem of drug resistance.
"Fecal Microbiota Transplantation" (FMT) is a novel treatment approach which involves
administration of feces from a healthy (donor) individual into a patient with relapsing CDI
to promote recolonization with missing components of normal intestinal flora. Numerous case
reports and retrospective case series have suggested benefit of FMT in patients with severe
or recurrent CDI with cure rates as high as 100% and a mean cure rate of 89% for the nearly
300 cases reported in the world literature. Although efficacy has been documented in these
case reports, to date there has not been a published prospective clinical trial of FMT for
CDI.
The proposed study would be the first randomized, double-blind, placebo (sham) controlled
clinical trial to determine whether FMT delivered at colonoscopy is effective at preventing
further relapse in patients who have suffered from at least a 3rd recurrence of CDI despite
receiving standard treatment. The investigators hypothesize that FMT is superior to placebo
in preventing relapse after treatment of CDI with vancomycin. As a result of this study, the
investigators will have preliminary efficacy data for this novel treatment approach for
recurrent CDI. The investigators will be better prepared to test the efficacy of FMT in
future multicenter clinical trials. This research will advance clinical care, potentially
impacting the protocol for treatment of relapsing C. difficile infection worldwide. This
proposal includes collaboration with an investigator capable of performing microbiome
analyses on specimens collected as part of the trial and will further understanding of the
intestinal microflora in health and disease.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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