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Research of plasma proteomics in patients with frequent exacerbations of chronic obstructive pulmonary disease(Fei-Pi Qi-Deficiency Syndrome) treated by Yiqigubiao pill

Research of plasma proteomics in patients with frequent exacerbations of chronic obstructive pulmonary disease(Fei-Pi Qi-Deficiency Syndrome) treated by Yiqigubiao pill

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007542
Enrollment
Unknown
Registered
2015-12-08
Start date
2016-03-01
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

Placebo group:According to the GOLD2011 recommended by the stability of the treatment program for treatment
At the same time, take YIqigubiao pill agent Simulation 10 each time, 3 times a day, 12 weeks.
Yiqigubiao pill group:According to the GOLD2011 recommended by the stability of the treatment program for treatment
At the same time, take YIqigubiao pill 10 each time, 3 times a day, 12 weeks

Sponsors

Traditional Chinese medicine hospital of Xinjiang Uygur Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients corresponding to diagnosis standards of stable COPD; (2) Patients corresponding to diagnosis standards of Fei-Pi Qi-Deficiency Syndrome; (3) Age from 40-75 years; (4) The survival period was more than 3 months; (5) Good compliance with the consent of the test, and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with Bronchial asthma, pulmonary tuberculosis, pulmonary tuberculosis, pulmonary cystic fibrosis, lung cancer, pulmonary abscess, congestive heart failure and other diseases; (2) Patients with serious cardiovascular, primary disease of liver, kidney, hematopoietic system; (3) Women in stage of pregnant or lactation; and Patients with psychosis; (4) Disabled patients (blind, deaf, mental retardation, physical disability); (5) People with multiple drug allergy of the test drug; patients with contraindications; (6) Patients with tumors; (7) People with congenital or acquired immunodeficiency; (8) Patients participate in other clinical trials in the recent month.

Design outcomes

Primary

MeasureTime frame
TCM symptom mark;COPD assessment test, CAT;Plasma proteomics research;

Secondary

MeasureTime frame
Pulmonary Function;the times and severity of exacerbation;

Countries

China

Contacts

Public ContactGao zhen
gaozhening@gmail.com+86 13565925717

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 27, 2026