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

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ClinicalTrials.gov Identifier: NCT00724919
Recruitment Status : Completed
First Posted : July 30, 2008
Last Update Posted : August 11, 2008
Sponsor:
Information provided by:
Wyeth is now a wholly owned subsidiary of Pfizer

Brief Summary:
To determine the acquisition rate of ESBL producing E. coli or K. pneumoniae, post- intervention in the selected medical centres

Condition or disease
Infection

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.

Study Type : Observational
Actual Enrollment : 256 participants
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)
Study Start Date : December 2003
Actual Primary Completion Date : April 2004
Actual Study Completion Date : April 2004

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Pneumonia

Group/Cohort
1



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

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


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
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


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

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

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