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The role and mechanism of respiratory microbiota homeostasis in chronic obstructive pulmonary disease with fungal infection

The role and mechanism of respiratory microbiota homeostasis in chronic obstructive pulmonary disease with fungal infection

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400083090
Enrollment
Unknown
Registered
2024-04-15
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

chronic obstructive pulmonary disease with fungal infection

Interventions

AECOPD/FI group:No intervention

Sponsors

The first affiliated hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Agree and sign an informed consent form, fully understand the research content, process, and potential adverse reactions; (2) Age = 40 years old, regardless of gender; (3) AECOPD patients meet the consensus of Chinese experts in the diagnosis and treatment of acute exacerbation of chronic obstructive pulmonary disease; (4) Patients with Aspergillus infection meet the diagnostic criteria of IDSA 2020 guidelines; (5) Broncho-pulmonary candidiasis meets the diagnostic criteria of the Chinese Expert Consensus on the Diagnosis and Treatment of Adult Candidiasis.

Exclusion criteria

Exclusion criteria: (1) Poor prognosis with an estimated survival time of less than 24 hours; (2) Pregnant and lactating women; (3) Concomitant autoimmune diseases; (4) Use oral corticosteroids or immunosuppressants within 2 weeks prior to admission; (5) Concomitant lack of granulocytes; (6) No use of antifungal drugs within 2 weeks prior to admission; (7) Active pulmonary tuberculosis; (8) Concomitant malignant tumors of the blood system or lungs; (9) Concomitant bronchial asthma; (10) Concomitant severe heart, liver, and kidney dysfunction; (11) Acute exacerbation of COPD after enrollment: (12) Patients who refuse to enter the study and are unable to obtain corresponding samples such as BALF and sputum; (13) Participate in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Abundance of microbiome;

Secondary

MeasureTime frame
CAT score;

Countries

China

Contacts

Public ContactZhi Ao

The first affiliated hospital of Chongqing Medical University

aozhi@cqmu.edu.cn+86 199 4233 0120

Outcome results

None listed

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