Central Line-Associated Bloodstream Infection QI Project | NCT07746674

NCT ID: NCT07746674
Lead Sponsor: NYU Langone HealthOTHER
Official Title: Central Line-Associated Bloodstream Infection (CLABSI) Quality Improvement Project
Brief Summary: This study evaluates a daily electronic health record (EHR) alert designed to reduce unnecessary central venous catheter (CVC) use among hospitalized adults. The alert identifies patients with an active CVC and no documented indication, prompting the first-contact provider to document line necessity. The study compares alert and a secure chat intervention to usual care, with the goal of reducing unnecessary line days and related CLABSI risk.
Conditions: Central Line-associated Bloodstream Infection (CLABSI)
Interventions: No data available

Participation Criteria

Ages Eligible for Study: Adult (18-64)Older Adult (65+)
Sexes Eligible for Study: All
Accepts Healthy Volunteers?: No
Eligibility Criteria: Inclusion Criteria:

Not hospice patient class

Active central line for at least 24 hours

Exclusion Criteria:

No active central line

Central line present for less than 24 hours

Study Type: Observational
Phase: No data available
Enrollment: 30Estimated
Primary Purpose: No data available
Allocation: No data available
Interventional Model: No data available
Masking: No data available
Masking Description: No data available
Observational Model: Cohort
Time Perspective: Prospective
Participant Group/Arms: Usual Care
Adult inpatients meeting eligibility criteria.
Secure Chat + Alert Cohort
Adult inpatients meeting eligibility criteria whose provider receives a daily EHR OPA alert and additional secure chat communication.

Central Contacts: Sarah TsuruoContact
Sarah.Tsuruo@nyulangone.org914-815-4079
Holly KrelleContact
Holly.Krelle@nyulangone.org347-200-1108
Locations: NYU Langone Health
New York, New York 10016, United States

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