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Clinical Trial Summary

Data on occurrence of antimicrobial resistant bacteria acquisition in rehabilitation centers will be collected. After removal of patient identifiers, information regarding the patients population will be entered into electronic sheet. The phase will last twelve months in each center.


Clinical Trial Description

All patients admitted to the department will be examined on admission, two weeks latter and monthly by obtaining nares and perirectal cultures. These cultures will be processed for detection the target organisms. This activity is part of the good medical practice and is performed on routine basis in various hospital units

Epidemiological data will be collected from patient records. This data will be stored after removal of all patients' identifiers. These data will be transferred for analysis to Tel Aviv Medical Center ;


Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Related Conditions & MeSH terms


NCT number NCT00773799
Study type Observational
Source Tel-Aviv Sourasky Medical Center
Contact yaffa lerman, MD
Phone 97252-4266910
Email yaffale@tasmc.health.gov.il
Status Not yet recruiting
Phase N/A
Start date October 2008
Completion date January 2014

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