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Clinical Study on Guben Kechuan Granules Promoting Disease Recovery by Regulating Immune-Inflammatory Dysregulation in Patients With Acute Exacerbation of Chronic Obstructive Pulmonary Disease During the Peri-Discharge Period

Clinical Study on Guben Kechuan Granules Promoting Disease Recovery by Regulating Immune-Inflammatory Dysregulation in Patients With Acute Exacerbation of Chronic Obstructive Pulmonary Disease During the Peri-Discharge Period

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001459
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Acute Exacerbation of Chronic Obstructive Pulmonary Disease During the Peri-Discharge Period

Interventions

Experimental group:Basic treatment with Guben Kechuan granule
Control group:Basic treatment with Placebo

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1: a. Meet the diagnostic criteria for Chronic Obstructive Pulmonary Disease (COPD), with lung function classified as Grade II-IV (Groups B and E), be in the peri-discharge period of Acute Exacerbation of COPD (AECOPD), and conform to the Traditional Chinese Medicine (TCM) syndrome of spleen deficiency with excessive phlegm and insecure kidney qi 2: b. Aged 40–75 years, regardless of gender 3: c. Inpatients 4: d. No prior use of Guben Kechuan Granules 5: e. Be willing to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1:   a. Patients with airflow limitation caused by other respiratory diseases such as bronchial asthma, bronchiectasis, pulmonary tuberculosis, and lung cancer 2:   b. Patients with severe concurrent diseases of the heart, brain, liver, kidney, etc., who are unable to cooperate with exercise 3:   c. Patients with impaired immune systems or those receiving long-term immunosuppressive therapy 4:   d. Patients currently participating in another interventional clinical trial of drugs or medical devices.

Design outcomes

Primary

MeasureTime frame
Degree of improvement in Forced Expiratory Volume in 1 second (FEV1);

Secondary

MeasureTime frame
COPD Assessment Test (CAT) Questionnaire;St. George's Respiratory Questionnaire (SGRQ) score;Modified Medical Research Council (mMRC) Dyspnea Questionnaire;6-Minute Walk Test (6MWT);C-reactive protein;WBC;T-lymphocyte;Indicators of inflammation;Transcriptome assays;Detection of serum metabolic profile;Lipidomic detection;

Countries

China

Contacts

Public ContactFeng Cuiling

Peking University People's Hospital

fengcuiling@sina.com15901341502

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 29, 2026