A Pilot of Pediatric/Adult Study of Gene Expression Profiling and Clinical Characterization of Phototoxicity
NCT00353158
Bacterial Infections, Bacterial Infections and Mycoses
Bethesda, Maryland, United States
View Trial DetailsNCT Number: NCT01788449
Assess efficacy of piperacillin/tazobactam in reducing the cases of colonization and infection of bacteria.
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Observational
Primarily, this study is designed to assess the efficacy of piperacillin/tazobactam in reducing the cases of colonization and infection of extended-spectrum betalactamases (ESBLs) producing E.coli or K pneumoniae, S aureus methicillin resistant (MRSA) and Enterococcus vancomycin resistant (VRE). Secondly, this study plans to determine the acquisition rate of ESBL producing E Coli or K pneumoniae, methicillin resistant S Aureus (MRSA) and vancomycin resistant Enterococcus spp (VRE), both pre- and post-intervention.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
All patients admitted in ICU will be enrolled (who qualify for treatment).
Time frame: 8 months
Time frame: 8 months
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Association of Antibiotic Measures and Control of Bacterial Resistance
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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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