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Study Evaluating Vancomycin-Resistant Enterococci in a Hematology Unit

Effects on the Emergence and Transmission of Vancomycin-Resistant Enterococci After Changes in Antibiotic Use in a Hematology Unit.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00167960
Enrollment
1500
Registered
2005-09-14
Start date
2005-01-31
Completion date
Unknown
Last updated
2007-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gram-Positive Bacterial Infections

Keywords

Bacterial Infections

Brief summary

To determine the impact of the restriction of the third and forth generation cephalosporins on the reduction of intestinal colonization or infection with vancomycin-resistant enterococci (VRE) in a surgical intensive care unit (SICU)

Interventions

DRUGPiperacillin/tazobactam and other β-lactam/β-lactamase

Sponsors

Wyeth is now a wholly owned subsidiary of Pfizer
Lead SponsorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients admitted to or transferred to the SICU. * Eligible patients will be patients of either sex, 18 years of age or older who are admitted or transferred to the SICU. * Provide written informed consent

Exclusion criteria

* Patients who have hypersensitivity to penicillin, cephalosporins or beta-lactamase inhibitors. * Females who are pregnant and breast feeding * Any underlying conditions or non-infectious diseases that will be ultimately fatal within 48 hours. * Those who have already been participating other clinical study related with antibiotics.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026