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The value of Fluconazole in refractory acute exacerbation of chronic obstructive pulmonary disease patients

The value of Fluconazole in refractory acute exacerbation of chronic obstructive pulmonary disease patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900025535
Enrollment
Unknown
Registered
2019-08-31
Start date
2019-10-08
Completion date
Unknown
Last updated
2019-09-02

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

Conditions

Acute Exacerbation of Chronic Obstructive Pulmonary Disease

Interventions

Experimental group and Control group:0.4mg Fluconazole injection Qd 5 days

Sponsors

Guangzhou 1st People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Male or Female patient aged above 40 years old; 2. Patients who meet the 2018 GOLD guidelines for COPD diagnosis, and who are in the acute exacerbation of moderate to severe COPD according to the GOLD guidelines; 3. Patients showed no improvement or worsen symptoms after 5 days standardized treatment (methylprednisolone 40mg / day, anti-infective, aerosolized bronchodilators and other comprehensive treatment) according to the GOLD guidelines; 4. Sign the written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Combined pneumonia, tuberculosis, lung cancer, bronchiectasis, interstitial lung disease, atelectasis, lung abscess, empyema, cystic fibrosis, granulomatous disease, obliterative bronchiolitis or recent pulmonary embolism, and pleural disease; 2. Myocardial infarction, unstable angina pectoris, grade 4 cardiac insufficiency, and decompensated pulmonary heart disease occurred in the past 3 months; 3. Severe liver and kidney failure, transaminase is more than 3 times the upper limit of reference range or creatinine clearance is less than 50 ml/min; 4. Identify fluconazole-resistant Candida infections, or other confirmed fungal infections other than Candida; 5. Organ transplantation or hematopoietic stem cell transplanters; 6. Immunosuppressive therapy is being used during chemotherapy or screening within 3 months prior to randomization. 7. Patients with absolute neutrophil counts <500/mm3; 8. Known HIV positive; 9. Women who are pregnant or breastfeeding, or women who plan to conceive or breastfeed during the study period. 10. Intolerant to azole according to the patient's medication history; 11. Pathogens that are not covered by antibiotics during the 5-day routine treatment and need to be adjusted.

Design outcomes

Primary

MeasureTime frame
Length of stay in hospital;

Countries

China

Contacts

Public ContactZiwen Zhao

Department of internal medicine, Guangzhou

zhaozw@yeah.net+86 13006872260

Outcome results

None listed

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