Gyunggi-do, 431-070, South Korea
NCT Number: NCT00167986
Study Evaluating Antibiotic Use in Reducing Vancomycin-Resistant Enterococci and ESBL Producing Escherichia Coli and Klebsiella Pneumoniae in Intensive Care
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 a medical intensive care unit (MICU).
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- All patients admitted to or transferred to the MICU.
- Patients 18 years of age or older.
- Provide written informed consent.
Exclusion criteria
- 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.
Treatment and study plan
vancomycin-resistant enterococci and ESBL
DrugSponsors and collaborators
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Registry information
Official study title
Antibiotic Intervention Trial in a Medical Intensive Care Unit to Reduce the Acquisition of Vancomycin-Resistant Enterococci and ESBL Producing Escherichia Coli and Klebsiella Pneumoniae.
Important dates
- Study start
- 2005
- First posted
- Sep 14, 2005
- Registry last updated
- Mar 15, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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