A Post-Intervention Surveillance Study Regarding the Acquisition Rate of ESBL-KP, Ecoli
NCT00724919
Last updated date
ABOUT THIS STUDY
To determine the acquisition rate of ESBL producing E. coli or K. pneumoniae, post-
intervention in the selected medical centres
FOR MORE INFORMATION
Contact a representative by phone, email, or visiting the study website. Please see the references below:
By phone
Pfizer Clinical Trials Contact Center
1-800-718-1021
Eligibility Criteria
condition
Infection
Sex
Females and Males
Age
18 + years
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Advanced Information
Descriptive Information | ||||
---|---|---|---|---|
Brief Title | A Post-Intervention Surveillance Study Regarding the Acquisition Rate of ESBL-KP, Ecoli | |||
Official Title | Association of Antibiotic Utilization Measures and Control of Extended-Spectrum ?-Lactamases (ESBLs) (A Post-Intervention Surveillance Study) | |||
Brief Summary | To determine the acquisition rate of ESBL producing E. coli or K. pneumoniae, post- intervention in the selected medical centres | |||
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 | |||
Study Design | Observational Model: Cohort Time Perspective: Prospective | |||
Target Follow-Up Duration | Not Provided | |||
Biospecimen | Not Provided | |||
Sampling Method | Non-Probability Sample | |||
Study Population | patients admitted to ICU/burn unit | |||
Condition | Infection | |||
Intervention | Not Provided | |||
Study Groups/Cohorts | 1 | |||
Publications * | Not Provided | |||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. | ||||
Recruitment Information | ||||
Recruitment Status | Completed | |||
Actual Enrollment | 256 | |||
Original Actual Enrollment | Same as current | |||
Actual Study Completion Date | April 2004 | |||
Actual Primary Completion Date | April 2004 (Final data collection date for primary outcome measure) | |||
Eligibility Criteria | Inclusion
Patients were excluded if they had underlying conditions or diseases that were ultimately fatal within 48 hours | |||
Sex/Gender |
| |||
Ages | 18 Years and older (Adult, Older Adult) | |||
Accepts Healthy Volunteers | No | |||
Contacts | Contact information is only displayed when the study is recruiting subjects | |||
Listed Location Countries | Taiwan | |||
Removed Location Countries | ||||
Administrative Information | ||||
NCT Number | NCT00724919 | |||
Other Study ID Numbers | 0910X-101440 | |||
Has Data Monitoring Committee | No | |||
U.S. FDA-regulated Product | Not Provided | |||
IPD Sharing Statement | Not Provided | |||
Responsible Party | Wyeth (Registry Contact: Clinical Trial Registry Specialist), Wyeth | |||
Study Sponsor | Wyeth is now a wholly owned subsidiary of Pfizer | |||
Collaborators | Not Provided | |||
Investigators |
| |||
PRS Account | Wyeth is now a wholly owned subsidiary of Pfizer | |||
Verification Date | August 2008 |