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A randomized controlled trial for the effect of Modified Shenling Baizhu Powder on delaying the illness progress of COPD stable phase patients (GOLD 1-2 stages).

A randomized controlled trial for the effect of Modified Shenling Baizhu Powder on delaying the illness progress of COPD stable phase patients (GOLD 1-2 stages).

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003887
Enrollment
Unknown
Registered
2020-09-02
Start date
2020-09-01
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

Chronic Obstructive Pulmonary Disease

Interventions

Sponsors

Department of Respiratory Medicine, Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients with a clinical diagnosis of stable COPD (GOLD stage 1-2); consistent with TCM lung qi deficiency syndrome; 2. No history of respiratory tract infection or acute exacerbation in the 4 weeks prior to randomization; 3. Those who are able to successfully perform pulmonary function measurements; 4. Patients are informed and sign written consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with chronic lung diseases in which intervention or treatment is required, such as interstitial lung diseasebronchial asthma, active tuberculosis, or bronchiectasis; 2. Patients with a combination of severe primary diseases, such as cardiovascular and cerebrovascular diseases, liver and kidney diseases, hematopoietic system diseases, endocrine diseases, severe mental disorders, malignant tumors; 3. Patients have evidence of alcohol or drug abuse, known or suspected allergy to the study drug or some of its components, and currently uses oral corticosteroids regularly; 4. Women who are breast-feeding, pregnant or expecting a child; 5. Patients who have been involved in any other clinical study in the past 6 months; 6. Patients unable to successfully use a DPI or perform pulmonary function measurements.

Design outcomes

Primary

MeasureTime frame
lung function;

Secondary

MeasureTime frame
St George's Respiratory Questionnaire;COPD acute exacerbations;COPD assessment test;modified British medical research council;

Countries

China

Contacts

Public ContactXiaohong Xie

Department of Respiratory Medicine, Hospital of Chengdu University of Traditional Chinese Medicine

xiaohong_xie1102@163.com+86 18908178521

Outcome results

None listed

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