Study on etiology of severe pneumonia based on high throughput sequencing of macro transcriptome

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000036293

Enrollment

Unknown

Registered

2020-08-22

Start date

2020-11-01

Completion date

Unknown

Last updated

2020-09-07

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

Conditions

Severe pneumonia

Interventions

case series:N/A

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. The selected subjects were admitted to the application unit and cooperative unit. According to the diagnostic criteria of cap guidelines in 2015, those who met the one main criteria or more than three secondary criteria were diagnosed as severe pneumonia. 2. The subjects who volunteered to participate in the study were willing to provide the necessary samples and signed the informed consent.

Exclusion criteria

Exclusion criteria: Excluding AIDS, organ transplantation and other immune dysfunction patients; excluding hepatitis B, tuberculosis and other long-term infection patients; excluding malignant tumor, severe liver and kidney dysfunction and other basic diseases.

Design outcomes

Primary

Measure	Time frame
Detection of respiratory pathogens;	—

Countries

China

Contacts

Public ContactZhang Yongzhen

Shanghai Public Health Clinical Center

zhangyongzhen@shphc.org.cn+86 18917456071

Outcome results

None listed

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