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Prospective cohort study on the treatment of chronic obstructive pulmonary disease with Zhi Chuan Ling oral solution

Research on the clinical positioning and therapeutic effect evaluation of Zhichuanling Oral Liquid in the treatment of Chronic obstructive Pulmonary Disease Based on systematic evaluation - expert argumentation - clinical verification

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2025001535
Enrollment
Unknown
Registered
2025-08-05
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-08-18

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

Exposure group:The treatment is guided by the guidelines for the combination of Zhichuan Ling Oral Liquid
Non-exposure group:Guidelines guide treatment

Sponsors

The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age: 40 to 75 years old (inclusive) gender not limited; (2) It meets the Western medical diagnostic criteria for COPD and is in a stable period; (3) Pulmonary function grade II to IV; (4) All the research subjects signed informed consent forms

Exclusion criteria

Exclusion criteria: (1) Those with severe primary and/or secondary respiratory diseases such as bronchial asthma and lung cancer; (2) Combined with other severe cardiovascular and cerebrovascular diseases malignant arrhythmias (including ventricular tachycardia atrial flutter uncontrolled rapid atrial fibrillation severe sinus tachycardia severe sick sinus node syndrome or third-degree atrioventricular block) glaucoma grade III or above benign prostatic hypertrophy urinary retention severe kidney diseases hematopoietic system diseases etc And mental patients (3) Those who are known to be allergic to this medicine or any other excipients (4) Those who do not meet the regulations for combined medication (5) Pregnant lactating women and women of childbearing age who have not adopted contraceptive plans.

Design outcomes

Primary

MeasureTime frame
The relief rate of cough symptoms in the second week after enrollment;

Secondary

MeasureTime frame
CAT score;mMRC dyspnea score;The hospitalization rate of patients in the second week of enrollment;Emergency visit rate;TCM syndrome score and individual symptom score;Pulmonary function;

Countries

China

Contacts

Public ContactFENG JIHONG

The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine

1194542291@qq.com13820337614

Outcome results

None listed

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