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Application of CCID chip rapid detection in severe pneumonia in ICU

Application of CCID chip rapid detection in severe pneumonia in ICU

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000038666
Enrollment
Unknown
Registered
2020-09-27
Start date
2020-09-28
Completion date
Unknown
Last updated
2020-12-14

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

Conditions

Severe pneumonia

Interventions

Gold Standard:Routine bacterial testing (traditional pathogenic testing methods)
Index test:Diagnosis&#32
of&#32
severe&#32
pneumonia
&#32
pathogen&#32
detection&#32
method
qualified&#32
deep&#32
sputum&#32
or&#32
bronchial&#32
lavage&#32
fluid&#32
and&#32
bacterial&#32
culture&#32

Sponsors

The First Hospital of Fuzhou
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria of severe pneumonia; 2. Patients in ICU.

Exclusion criteria

Exclusion criteria: 1. Patients with severe infection of other organs; 2. Patients in ICU within 3 days after admission.

Design outcomes

Primary

MeasureTime frame
Pathogenic microorganisms;—

Countries

China

Contacts

Public ContactSu Huangcai

The First Hospital of Fuzhou

suhuangcai@163.com+86 13960904289

Outcome results

None listed

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