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The effect of clinical application of closed sputum specimen collection device on prevention of microbial contamination in intensive care unit

Effect of clinical application of closed sputum specimen collection device on prevention of microbial contamination in intensive care unit

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038199
Enrollment
Unknown
Registered
2020-09-13
Start date
2020-10-09
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

Patients with severe pneumonia

Interventions

experimental group:Closed device
control group:Open device

Sponsors

Children's Hospital, Capital Institute of Paediatrics
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: Informed consent has been signed to participate in the study of bacterial pneumonia patients, who need ventilator with tracheal intubation, duration of ventilation support > 3 days .(OI<250mmHg)

Exclusion criteria

Exclusion criteria: Nil

Design outcomes

Primary

MeasureTime frame
colony forming unit;—

Secondary

MeasureTime frame
SPO2;HR;BP;TV;PIP;PEEP;Cdyn;—

Countries

China

Contacts

Public ContactLinying Guo

Emergency Department, Children's Hospital, Capital Institute of Pediatrics

13020013651@163.com+86 13020013651

Outcome results

None listed

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