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Clinical study of Wenshen Yiqi Granules in improving airway hypersecretion in patients with chronic obstructive pulmonary disease

Clinical study of Wenshen Yiqi Granules in improving airway hypersecretion in patients with chronic obstructive pulmonary disease

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100004267
Enrollment
Unknown
Registered
2020-10-15
Start date
2020-10-31
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

COPD

Interventions

Sponsors

The Second Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. It meets the diagnostic criteria of the Chronic Obstructive Pulmonary Disease Global Initiative 2013 Edition, and the forced expiratory volume in the first second after inhalation of bronchodilator accounts for the percentage of the predicted value (FEV1 accounts for the predicted value%) between 30% and 79%; 2. Comply with the diagnostic criteria of lung and kidney qi deficiency in the Diagnosis and Curative Effect Criteria for TCM Diseases; 3. In a stable period, no respiratory infection and acute attack of chronic obstructive pulmonary disease in the past 4 weeks; 4. Have at least 2 history of acute exacerbations or one hospitalization for acute exacerbations in the past year; 5. No other treatments were used before treatment, and no other drug clinical research was taken within one month; 6. Accept the experimental research voluntarily and sign an informed consent form. The informed consent process complies with ethical requirements.

Exclusion criteria

Exclusion criteria: 1. Asthma or other non-chronic obstructive pulmonary diseases caused by airway obstruction; 2. Patients with severe primary diseases and mental illnesses such as cardiovascular, liver, kidney and hematopoietic system; 3. Pregnant or lactating women; 4. Those who are allergic to the study drug; 5. Those who are unwilling to accept research measures or cannot cooperate for other reasons.

Design outcomes

Primary

MeasureTime frame
MUC5AC;TNF-a;IL-8;

Countries

China

Contacts

Public ContactLiyan Qian

The Second Affiliated Hospital of Zhejiang Chinese Medical University

orange.1211@163.com+86 13958135148

Outcome results

None listed

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