Improving prevention of catheter-related bloodstream infections in ICUs

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This multicenter clinical trial aims to implement and evaluate a continuous quality improvement project called 'ICU-NO CRBSI' to prevent catheter-related bloodstream infections (CRBSI) in intensive care units. The study involves a cluster-randomized controlled design across 23 medical institutions, focusing on compliance with evidence-based practices for central venous catheter care. Participants will be monitored over several months to assess the effectiveness of the intervention and the necessary support for quality improvement. The study will analyze the incidence of CRBSI and adherence to prevention protocols among healthcare providers.

Why it matters

Who can join: the full rules

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

Where it's running

• ZhongShan Hospital Affilicated to Fudan University
  Shanghai, Shanghai Municipality, China Recruiting

Study contacts

• Study coordinator: CHUNLEI Li
• Email: 21211170023@m.fudan.edu.cn
• Phone: 15800488689

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.