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A Post-Intervention Surveillance Study Regarding the Acquisition Rate of ESBL-KP, Ecoli

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00724919
First Posted: July 30, 2008
Last Update Posted: August 11, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Wyeth is now a wholly owned subsidiary of Pfizer
  Purpose
To determine the acquisition rate of ESBL producing E. coli or K. pneumoniae, post- intervention in the selected medical centres

Condition
Infection

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Association of Antibiotic Utilization Measures and Control of Extended-Spectrum β-Lactamases (ESBLs) (A Post-Intervention Surveillance Study)

Resource links provided by NLM:


Further study details as provided by Wyeth is now a wholly owned subsidiary of Pfizer:

Primary Outcome Measures:
  • The acquisition rate of ESBL producing E. coli or K. pneumoniae at the end of surveillance phase [ Time Frame: 48hours ]

Secondary Outcome Measures:
  • The infection rate due to ESBL producing E. coli, or due to K. pneumoniae at the end of surveillance phase [ Time Frame: 48hours ]

Enrollment: 256
Study Start Date: December 2003
Study Completion Date: April 2004
Primary Completion Date: April 2004 (Final data collection date for primary outcome measure)

Detailed Description:
This is post-interventional study to follow the acquisition rate of ESBP producing E. coli or K. pneumoniae at the sites involved in a previous interventional study.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
patients admitted to ICU/burn unit
Criteria

Inclusion

  1. All patients admitted or transferred to ICU/burn unit.
  2. Patients of either sex, 18 years of age or older. Exclusion

Patients were excluded if they had underlying conditions or diseases that were ultimately fatal within 48 hours

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00724919


Locations
Taiwan
Miaoli County, Taiwan, 351
Taichung, Taiwan, 40705
Sponsors and Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer
Investigators
Study Director: Medical Monitor Wyeth is now a wholly owned subsidiary of Pfizer
  More Information

Responsible Party: Wyeth (Registry Contact: Clinical Trial Registry Specialist), Wyeth
ClinicalTrials.gov Identifier: NCT00724919     History of Changes
Other Study ID Numbers: 0910X-101440
First Submitted: July 23, 2008
First Posted: July 30, 2008
Last Update Posted: August 11, 2008
Last Verified: August 2008

Keywords provided by Wyeth is now a wholly owned subsidiary of Pfizer:
ESBL