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Yi Huo Hua Tan granule for the treatment of stable chronic obstructive pulmonary disease (qi deficiency syndrome with phlegm and blood stasis obstructing the lung)

Yi Huo Hua Tan granule for the treatment of stable chronic obstructive pulmonary disease (qi deficiency syndrome with phlegm and blood stasis obstructing the lung)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16010038
Enrollment
Unknown
Registered
2016-11-29
Start date
2017-07-01
Completion date
Unknown
Last updated
2017-04-18

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

Experimental Group:Yi Huo Hua Tan granule

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosis of stable COPD according to western medicine; (2) Diagnosis of qi deficiency syndrome with phlegm and blood stasis obstructing the lung according to TCM; (3) Aged between 45 and 80 years old; (4) Signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Chronic cough and wheeze caused by tuberculosis, tumour, irritant gas or anaphylactic reaction; (2) Patients with serious primary diseases of cardiovascular, liver, kidney and hematopoietic system; (3) Chronic bronchitis complicated with acute cardiac insufficiency; (4) Behavior or mental illness; (5) Allergic constitution; (6) patients who can not use the drug according the plan or whose information in not complicated; (7) Participanting in other drug clinical trials.

Design outcomes

Primary

MeasureTime frame
Number of exacerbations in last 12 months;

Secondary

MeasureTime frame
CAT;mMRC;CCQ;6MWT;SGRQ;HADS;Lung function test;TCM score;Plasma inflammation cytokines;Induced sputum inflammation cytokines;

Countries

China

Contacts

Public ContactBing Mao

West China Hospital of Sichuan University

maobing@medmail.com.cn+86 18980601724

Outcome results

None listed

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