Status:

COMPLETED

Study Evaluating Antibiotic Use in Reducing Vancomycin-Resistant Enterococci and ESBL Producing Escherichia Coli and Klebsiella Pneumoniae in Intensive Care

Lead Sponsor:

Wyeth is now a wholly owned subsidiary of Pfizer

Conditions:

Escherichia Coli Infections

Klebsiella Infections

Eligibility:

All Genders

18+ years

Brief Summary

To determine whether the restriction of 3rd generation cephalosporins and carbapenems contribute to the reduction of intestinal colonization or infection with vancomycin-resistant enterococci (VRE) in...

Eligibility Criteria

Inclusion

  • All patients admitted to or transferred to the MICU.
  • Patients 18 years of age or older.
  • Provide written informed consent.

Exclusion

  • Patients known to be infected or colonized by VRE or ESBL-producing E.coli, K.pneumoniae.
  • Patients who have hypersensitivity to penicillin.
  • Any underlying conditions or diseases that will be ultimately fatal within 48 hours.
  • Any concurrent condition or medication which would interfere with absorption or metabolism of study drugs.

Key Trial Info

Start Date :

January 1 2005

Trial Type :

OBSERVATIONAL

End Date :

Estimated Enrollment :

480 Patients enrolled

Trial Details

Trial ID

NCT00167986

Start Date

January 1 2005

Last Update

March 15 2007

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

Gyunggi-do, South Korea, 431-070