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An observational study on the application of BLUE-plus protocol in critical care patients

An observational study on the application of BLUE-plus protocol in critical care patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-DDD-17012391
Enrollment
Unknown
Registered
2017-08-16
Start date
2017-09-01
Completion date
Unknown
Last updated
2017-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

respiratory failure

Interventions

Gold Standard:Routine
Index test:lung&#32
ultrasound&#32
screening&#32
following&#32
the&#32
BLUE-plus&#32
protocol

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) ICU patients aged =18 years; (2) Stay in ICU =24 hours.

Exclusion criteria

Exclusion criteria: (1) younger than 18 years old; (2) could not change positions because of severe hemodynamic instability; (3) could not obtain the LUS images because of severe chest deformity or massive subcutaneous emphysema; (4) did not obtain the LUS images of all the 10 BLUE-plus points; (5) the final etiology is undiagnosed.

Design outcomes

Primary

MeasureTime frame
sensitivity;specificity;Positive predictive value ;negative predictive value ;Area under ROC curve;—

Countries

China

Contacts

Public ContactLi-Na Zhang

Xiangya Hospital, Central South University

zln7095@163.com+86 15874875763

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026