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A clinic test between airway microbiota and lung injury in sepsis patients

A clinic test between airway microbiota and lung injury in sepsis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096719
Enrollment
Unknown
Registered
2025-02-05
Start date
2023-12-02
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

Sepsis

Interventions

Sepsis group:None
control group:None

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients who undergo tracheal intubation within the ICU or are intubated within 24 hours after intubation, have no evidence of pneumonia before admission (i.e. no new or ongoing complications), and have an estimated intubation time of>96 hours, aged 18-90 years, are divided into sepsis group and non sepsis group based on whether they meet the diagnostic criteria for sepsis (infection+SOFA score>2 points).

Exclusion criteria

Exclusion criteria: Expected to take less than 96 hours of tubing; Under 18 years old; Pregnancy or lactation period; Expected circulatory respiratory failure requiring rescue; Evaluate patients who cannot tolerate sputum suction; Patients with lung injury caused by aspiration, chest trauma, or other reasons before the start of mechanical ventilation; Patients who continuously take antibiotics before mechanical ventilation; Individuals with a history of chronic pulmonary infections; Long term consumption of probiotic products; Patients with acute or chronic respiratory infections, mutations, trauma, and other diseases.

Design outcomes

Primary

MeasureTime frame
Airway microbiota;

Secondary

MeasureTime frame
oxygenation index;blood gas analysis;

Countries

China

Contacts

Public ContactKeliang Xie

Tianjin Medical University General Hospital

55358645@qq.com+86 153 3211 2099

Outcome results

None listed

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