The Causes and Interpretation of Low-level Resistance in Staphylococcus Aureus
1 other identifier
observational
45
1 country
1
Brief Summary
The hypothesis of this investigation is that rate of isolation of resistant nosocomial pathogens can be explained by a combination of measures that include, among other things, antimicrobial drug use, infection control efforts, patient mix and antimicrobial stewardship efforts. The short term goal of this investigation is to improve our understanding of the relationships between antimicrobial stewardship program efforts (and actual antimicrobial drug use), and infection control efforts to the incidence rates of MSSA, MRSA, h-VISA and SA-MICcreep. The long term goal of this investigation is to design interventions that will improve antimicrobial drug use and decrease cross-transmission of resistant bacteria, resulting in a decrease in the rates of infection caused resistant hospital organisms.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Apr 2010
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2010
CompletedFirst Submitted
Initial submission to the registry
May 19, 2010
CompletedFirst Posted
Study publicly available on registry
May 21, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2013
CompletedJuly 9, 2014
July 1, 2014
3.1 years
May 19, 2010
July 8, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Proportion of hospitals that test for MIC creep to vancomycin
Survey of hospitals participating in the UHC consortium
2009
Eligibility Criteria
Adult inpatients
You may qualify if:
- Adult inpatients
You may not qualify if:
- Pediatric inpatients
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Virginia Commonwealth Universitylead
- Astellas Pharma Inccollaborator
Study Sites (1)
Virginia Commonwealth University School ofPharamcy
Richmond, Virginia, 23298, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- ECOLOGIC OR COMMUNITY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 19, 2010
First Posted
May 21, 2010
Study Start
April 1, 2010
Primary Completion
May 1, 2013
Study Completion
May 1, 2013
Last Updated
July 9, 2014
Record last verified: 2014-07