Evaluation of Body-worn Multimodal Hand Hygiene System. Impact on Health-Care Associated Infections
Sprixx-ICU
Real Time Deployment of Multimodal Personal Dispenser Hand Hygiene System in a Multidisciplinary Intensive Care Unit.
1 other identifier
observational
2,954
1 country
1
Brief Summary
Evaluate the efficacy of a multimodal hand hygiene system in the intensive care unit environment and evaluate any impact on health care associated infections.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2007
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
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2009
CompletedFirst Submitted
Initial submission to the registry
January 14, 2010
CompletedFirst Posted
Study publicly available on registry
January 15, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2011
CompletedJune 23, 2011
June 1, 2011
2 years
January 14, 2010
June 22, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Reduction in healthcare associated infections (CRBSI and VAP)
2 years
Secondary Outcomes (1)
Time to infections Hospital mortality Length of stay
2 years
Study Arms (2)
Sprixx Device Group
Treatment group utilizing multimodal hand hygiene device
Standard Hand Hygiene Group
Utilizing wall mounted dispensers and CDC based guidelines.
Interventions
Records hand hygiene events of provider and tabulates on the group level.
CDC based guidelines with regard to utilization in the health care environment "the nest"
12 minute education prior to deploying device for all providers.
Provide feedback with regard to expected hand hygiene goals to providers and reported anonymous group results based on recorded information.
Eligibility Criteria
Intensive Care Unit Patients Multidisciplinary Intensive Care Unit
You may qualify if:
- All ICU patients
You may not qualify if:
- Patient is not in an ICU at our Institution
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dartmouth-Hitchcock Medical Centerlead
- Harbor Medical Inc.collaborator
Study Sites (1)
Dartmouth-HItchcock Medical Center
Lebanon, New Hampshire, 03756, United States
Related Publications (1)
Anesthesiology 2008; 109 A54 ASA Abstracts
RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Matthew D. Koff, M.D. M.S.
Dartmouth-Hitchcock Medical Center
- PRINCIPAL INVESTIGATOR
Randy L Loftus, M.D.
Dartmouth-Hitchcock Medical Center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
January 14, 2010
First Posted
January 15, 2010
Study Start
December 1, 2007
Primary Completion
December 1, 2009
Study Completion
January 1, 2011
Last Updated
June 23, 2011
Record last verified: 2011-06