Skip to content

Randomized Controlled Clinical Trial of Bushen Fangchuan Tablets in the Intervention of Asthma-COPD Overlap in Stable Phase with Lung and Kidney Deficiency

Randomized Controlled Clinical Trial of Bushen Fangchuan Tablets in the Intervention of Asthma-COPD Overlap in Stable Phase with Lung and Kidney Deficiency

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000755
Enrollment
Unknown
Registered
2026-03-27
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Asthma-COPD Overlap

Interventions

Basic treatment + Kidney-Strengthening and Asthma-Preventing Tablets:ICS/LABA/LAMA + Tonifying Kidney and Preventing Asthma Tablets
2) Basic treatment + Shenxiang Anti-Cough Tablets (placebo):ICS/LABA/LAMA + Tonifying Kidney and Preventing Asthma Tablets placebo

Sponsors

Kashi City People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1) Age range: 40 years old to 85 years old (gender not restricted); 1) Weight range: 45 kilograms to 85 kilograms; 2) According to diagnostic criteria, those meeting the ACO criteria; 3) Stable patients without significant worsening of cough or expectoration symptoms; 4) Pulmonary function test results meeting the moderate and severe obstruction criteria of 30 = FEV1%pred < 80; 5) Patients diagnosed with the syndrome of lung and kidney deficiency by traditional Chinese medicine; 6) Without cognitive, speech disorders or mental system diseases, and able to cooperate with the completion of the clinical study; 7) Participants voluntarily participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Exclude patients with other severe diseases of the lungs, heart, liver, kidneys and blood system (such as pulmonary heart disease, malignant tumors, respiratory failure and pneumothorax, etc.). 2) Patients with severely impaired heart, liver, kidney functions: cardiac function grade 3-4, ALT and/or AST exceeding 1.5 times the upper limit of normal, and Cr exceeding the upper limit of normal. 3) Exclude patients in the acute exacerbation stage of chronic obstructive pulmonary disease. 4) Pregnant or planning to become pregnant, lactating women. 5) Patients using concomitant medications, especially those that have a significant impact on the test drug, affecting the judgment of its efficacy and safety. 6) Those who participated in other clinical studies within the previous 4 weeks. 7) Other situations that the investigator deems unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
ACT(Asthma Control Test);CAT(COPD Assessment Test);

Secondary

MeasureTime frame
Pulmonary function;mMRC;Quantitative scoring of TCM syndromes;Acute exacerbation situation;

Countries

CHINA

Contacts

Public ContactJingcheng Dong

Fudan University Institute of Integrated Traditional Chinese and Western Medicine

jcdong2004@126.com13601761761

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026