Status:
NOT_YET_RECRUITING
Evaluating the Efficacy and Safety of Modified Qing-Zao-Jiu-Fei Decoction on Pneumoconiosis Patients
Lead Sponsor:
Chinese University of Hong Kong
Conditions:
Pneumoconiosis
Eligibility:
All Genders
20-85 years
Phase:
PHASE2
Brief Summary
This is a multicenter, randomized, double-blind, placebo-controlled study to investigate the beneficial efficacy and safety of Chinese medicine formula Modified Qing Zao Jiu Fei Decoction (MQZJFD) on ...
Eligibility Criteria
Inclusion
- Inclusion criteria
- Aged 20-85;
- Patients with pneumoconiosis (Confirmed case of pneumoconiosis by Pneumoconiosis compensation fund board);
- Agree to undergo blood test and willing to complete questionnaires and take medication as scheduled; and
- Willing to provide written informed consent.
- Exclusion criteria
- Patient with the following Chinese medicine syndromes/patterns according to Chinese medicine theory: dampness, lung deficiency and coldness, or Yang deficiency according to Chinese medicine theory;
- Patients receiving Chinese medicine in a regular pattern within the past 2 weeks;
- Patients with chronic co-morbidities such as other fibrotic lung diseases in addition to pneumoconiosis and/or co-existing heart disease;
- Patients with a medical history of malignancy within the past 5 years;
- Patients with a medical history of any serious diseases such as severe kidney and liver impairments, autoimmune disease, thyroid disease, Hodgkin's disease, lymphoma and leukemia;
- Patients with known severe cognitive and mental disorders;
- Documented pregnancy or lactation; or
- Patients allergic to the drug used in this study.
Exclusion
Key Trial Info
Start Date :
November 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 30 2027
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT07178184
Start Date
November 1 2025
End Date
April 30 2027
Last Update
September 17 2025
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