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Clinical Trial Summary

In this record review study, our objective is to determine the rates of cure, failure and relapse following treatment of C. difficile colitis with metronidazole.


Clinical Trial Description

Clostridium difficile is a major cause of nosocomial infection. When this organism proliferates in the colon, usually as a result of prior antibiotic therapy in a hospitalized or otherwise debilitated person, a variety of potentially serious consequences follow, such as fever, leukocytosis, abdominal pain, diarrhea and ileus. Some patients require surgical exploration and colectomy, and our hospital has had several deaths attributable to C. difficile colitis in the past year.

C. difficile colitis is treated with metronidazole, and earlier literature on this subject, written in the 1980's and early 1990s, suggests that the response rate is excellent, exceeding 90-95%. Our clinical observation has suggested that treatment with metronidazole is followed by a surprisingly high rate of failure, perhaps 25-30%. The clinical problem is that there are, at present, no desirable alternatives. Vancomycin, given orally, is said to be highly effective in treating this infection, but this may not be true, and the administration of this drug is associated with emergence of vancomycin-resistant bacteria, a major problem in modern hospitals. No other drug is approved for treatment of C. difficile infection.

We believe it is important to determine the actual rate of failure of treatment with metronidazole. This will provide an impetus for developing new therapeutic approaches.

We will review the records of patients who have been treated for confirmed C. difficile infection with metronidazole at the VAMC for the past 12 months in order to determine the rates of cure, failure, and relapse following therapy. This is a simple record review study to determine if our clinical suspicion is correct, namely, if the rate of failure of metronidazole therapy is much higher than that reported in the medical literature of 10-15 years ago. ;


Study Design

N/A


Related Conditions & MeSH terms


NCT number NCT00304369
Study type Observational
Source VA Medical Center, Houston
Contact
Status Completed
Phase N/A
Start date June 2005
Completion date June 2007

See also
  Status Clinical Trial Phase
Completed NCT00382304 - A Study of the Absorption of GT267-004 in Patients With Clostridium Difficile-Associated Diarrhea Phase 2
Completed NCT00304876 - Fecal Bacterial Flora in Clostridium Difficile-Associated Diarrhea N/A
Completed NCT03427229 - Fecal Microbiota Transplantation for Severe Clostridium Difficile Infection Phase 2
Completed NCT00106509 - A Study of GT267-004 Versus Vancomycin and GT267-004 Versus Metronidazole in Patients With C.Difficile - Associated Diarrhea Phase 3
Completed NCT00304889 - Vancomycin vs. Nitazoxanide to Treat Recurrent C. Difficile Colitis Phase 3
Completed NCT00304408 - Association Between Response to Treatment of C. Diff Colitis and Anti-C.Diff Toxin Antibody Phase 4
Completed NCT00304356 - Compassionate Use of Nitazoxanide for the Treatment of Clostridium Difficile Infection Phase 3
Completed NCT00182429 - Efficacy of Metronidazole Versus Metronidazole and Rifampin in CDAD Treatment Phase 3
Withdrawn NCT00304863 - Addition of Lactobacillus to Metronidazole in Treatment of CDAD Phase 4