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A prospective cohort study of the efficacy and outcome of GOLD treatment regimens for patients with different airway microbial types of chronic obstructive pulmonary disease

A prospective cohort study of the efficacy and outcome of GOLD treatment regimens for patients with different airway microbial types of chronic obstructive pulmonary disease

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-17012653
Enrollment
Unknown
Registered
2017-09-13
Start date
2017-11-01
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

COPD

Interventions

Bacillus group:Drugs
Cocci group:Drugs
Spiral bacteria group:Drugs

Sponsors

The Affiliated Hospital of Guangdong Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1. aged 40-79 years male and female; 2. with cough, sputum or dyspnea and other symptoms, chest imaging with emphysema performance, lung function criteria include: inhalation of bronchodilator FEV1 / FVC ratio = 70%; 3. without respiratory infection and acute exacerbation of COPD in past four weeks; 4. 30 days before screening, no antibiotics were used; 5. GOLD assessed as B or C patients.

Exclusion criteria

Exclusion criteria: 1. patients with COPD in addition to other respiratory diseases, such as asthma, asthma, interstitial pneumonia, active tuberculosis, community-acquired pneumonia, lung cancer, bronchiectasis, pulmonary heart disease, pulmonary embolism; 2. patients with grade C need to be combined with ICS 3. 30 days before screening, patients used antibiotics; 4. Patients with alcohol or narcotic drug abuse, drug history, or psychiatric history (such as schizophrenia, obsessive-compulsive disorder, depression), confrontation, negative motives, suspicion or other emotional or intellectual problems may affect participation in this study Effectiveness of the situation; 5. is participating in other drug clinical trial project, or stop time is less than 3 months; 6. patients induced sputum culture as a fungus or virus infection or its airway micro-ecological detection does not meet the bacilli, cocci or spiral group of patients; 7. patients can not cooperate with the relevant inspection of the project, do not agree to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Lung function;

Secondary

MeasureTime frame
The frequency of acute exacerbations of the past year;

Countries

China

Contacts

Public ContactBin Wu

The Affiliated Hospital of Guangdong Medical University

wub621011@126.com+86 13590090068

Outcome results

None listed

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