Association Between Response to Treatment of C. Diff Colitis and Anti-C.Diff Toxin Antibody
Completed
Conditions studied: Clostridium Enterocolitis, Pseudomembranous Colitis, Antibiotic-Associated Colitis
In brief
The purpose of this study is three fold: 1)To collect serum from patients with documented Clostridium difficile infection and test for the presence of antibody to C. difficile toxin at the start and at the end of therapy, and again if a relapse or recurrence occurs. 2)To collect stool samples for test of C. difficile toxin at similar time intervals. 3)To assay random serum samples from the VA lab in order to determine the rate of antibody to C. difficile toxin in our patient population.
Key facts
- Study ID
- NCT00304408
- Run by
- Michael E. DeBakey VA Medical Center
- People needed
- 10
- Starts
- 2005-01-01
- Expected to finish
- 2008-01-01
- Last updated by the study team
- 2010-09-10
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All patients at the Houston VA with documented C. difficile infection
You may not qualify if…
- None
Where it is running
- Michael E. Debakey VA Medical Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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