Multicenter Clinical Translational Study of "ICU-NO CRBSI" Based on Improvement Science
Recruiting
N/A
Interventional Study
CRBSI - Catheter Related Bloodstream Infection
Evidence-based Nursing Practice
Central Venous Catheter Related Bloodstream Infection
Central Venous Catheter Associated Bloodstream Infection
Central Line Infection
CLABSI - Central Line Associated Bloodstream Infection
Quality Improvement
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 8,050 (estimated)
- Sponsor
- Fudan University · Other
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About This Trial
The goal of this type of study is to construct the continuous quality promotion project "ICU-NO CRBSI(Catheter-Related Bloodstream Infection , CRBSI)" based on improvement science, and to verify its effect in the prevention of central venous catheter-related bloodstream infection and continuous quality improvement in ICU ( Intensive Care Unit , ICU) through multi-center implementation and two roun…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* ICU stay over 48 hours
* CVC was placed for more than 24 hours
Exclusion Criteria:
* Pregnant patients
* Patients with a history of CRBSI infection
* Patients with central venous catheterization were brought in from other hospitals
Contacts