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Clinical Trial Summary

The use of LGG will be associated with elimination of VRE colonization. The primary comparison will be VRE elimination rates among those patients that receive LGG compared to those that receive placebo. The primary endpoint will be the proportion of patients with VRE at one week after cessation of administration of study medication or placebo. The investigators assume that the placebo group will have very little spontaneous elimination of VRE and that the LGG group will be more likely to have eliminated VRE colonization at the end of one week.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Vancomycin Resistant Enterococcal Colonization

NCT number NCT00756262
Study type Interventional
Source Tufts Medical Center
Contact
Status Terminated
Phase Phase 1
Start date March 2003
Completion date July 2012