Multicenter Clinical Translational Study of "ICU-NO CRBSI" Based on Improvement Science

NCT06085690 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8050

Last updated 2025-11-17

No results posted yet for this study

Summary

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 rounds of improvement.

The main question\[s\] it aims to answer are:

What is the incidence of catheter-related bloodstream infection in the ICU of participating units? How compliant are health care providers in the ICU with evidence-based sensory control practices for the prevention of catheter-associated bloodstream infection?

Participants will be provided with the hospital's routine CVC (Central Venous Catheter ,CVC) care practices and CVC quality improvement measures based on evidence-based guidelines What technical and cultural support is needed to implement quality and safety improvement measures?

Conditions

  • 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

Interventions

BEHAVIORAL

evidence-based intervention Plan for the Prevention of CRBSI in ICU patients

On the basis of routine nursing, the "evidence-based intervention Plan for the Prevention of CRBSI in ICU patients" was implemented for intervention.

Sponsors & Collaborators

  • Fudan University Evidence-based Nursing Center

    collaborator UNKNOWN
  • Shanghai Zhongshan Hospital

    collaborator OTHER
  • Children's Hospital of Fudan University

    collaborator OTHER
  • Shanghai Public Health Clinical Center

    collaborator OTHER_GOV
  • Shandong First Medical University affiliated Provincial Hospital

    collaborator UNKNOWN
  • Affiliated Hospital of Nantong University

    collaborator OTHER
  • Hospital of Obstetrics and Gynecology affiliated to Fudan University

    collaborator UNKNOWN
  • Shengjing Hospital

    collaborator OTHER
  • The First Affiliated Hospital of University of South China

    collaborator OTHER
  • East China Hospital Affiliated to Fudan University

    collaborator UNKNOWN
  • The First Affiliated Hospital of Dali University

    collaborator UNKNOWN
  • Xinjiang Bayingoleng Mongolian Autonomous Prefecture People's Hospital

    collaborator UNKNOWN
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • Chinese Academy of Medical Sciences

    collaborator OTHER
  • Shanghai Minhang Central Hospital

    collaborator OTHER
  • Xi 'an children's hospital

    collaborator UNKNOWN
  • Huashan Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Xi 'an Jiaotong University

    collaborator UNKNOWN
  • Affiliated Hospital of Guizhou Medical University

    collaborator UNKNOWN
  • Affiliated Hospital of Southwest Medical University

    collaborator OTHER
  • Shenzhen Third People's Hospital

    collaborator OTHER
  • Shanghai Dongfang Hospital

    collaborator UNKNOWN
  • Fudan University

    lead OTHER

Principal Investigators

  • Yan Hu · School of Nursing, Fudan University; Center for Evidence-based Nursing, Fudan University

  • YuXia Zhang · Department of Nursing, Zhongshan Hospital Affiliated to Fudan University

  • Ying Gu · Center for Evidence-based Nursing, Fudan University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-09-04
Primary Completion
2025-09-30
Completion
2025-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06085690 on ClinicalTrials.gov