Piperacillin as a Part of Antibiotic Streamlining in the Intensive Care Unit
1 other identifier
observational
1,000
1 country
1
Brief Summary
The proposed endpoints of the study would be: comparative use of piperacillin versus broader spectrum agents (e.g., piperacillin/tazobactam, etc.) \[measured as defined daily doses per 1000 patient days\]; physician acceptance of piperacillin as part of a streamlining program \[measured as successful occurrences of the use of piperacillin as streamlining therapy\]; changes in susceptibility patterns of broad spectrum antibiotics \[measured as % Gram negative bacilli susceptible to each of the commonly used broad spectrum antibiotics\]; and outcome of patients treated with streamlined therapy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2005
Longer than P75 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
September 1, 2005
CompletedFirst Submitted
Initial submission to the registry
September 13, 2005
CompletedFirst Posted
Study publicly available on registry
September 15, 2005
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2017
CompletedJune 12, 2018
June 1, 2018
11.8 years
September 13, 2005
June 11, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
dead or alive
health status
end of study
Eligibility Criteria
patients treated with piperacillin/tazobactam and or piperacillin
You may qualify if:
- Patients with Gram negative infections treated with piperacillin/tazobactam and/or piperacillin
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Pittsburghlead
- Celgene Corporationcollaborator
Study Sites (1)
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, 15213, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
David Paterson, MD
University of Pittsburgh
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 13, 2005
First Posted
September 15, 2005
Study Start
September 1, 2005
Primary Completion
June 1, 2017
Study Completion
June 1, 2017
Last Updated
June 12, 2018
Record last verified: 2018-06