Ancient herbs take on black lung: new trial tests traditional remedy
NCT ID NCT07178184
First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tests whether a mix of 11 Chinese herbs, called Modified Qing-Zao-Jiu-Fei Decoction, can help people with pneumoconiosis (a lung disease from inhaling dust). Eighty adults aged 20-85 will receive either the herb granules or a placebo for 16 weeks. The main goal is to see if the herbs improve how far they can walk in 6 minutes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Modified Qing-Zao-Jiu-Fei Decoction (a mix of 11 Chinese herbs)
- What this could lead to
- If it works, this could offer a new way to help people with pneumoconiosis breathe easier and walk farther.
- What could go wrong
- This is a small, early-phase trial with only 80 people. The herbal mix may not work better than placebo, and side effects are possible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2025
An estimate. Start dates often move.
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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20 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria 1. Aged 20-85; 2. Patients with pneumoconiosis (Confirmed case of pneumoconiosis by Pneumoconiosis compensation fund board); 3. Agree to undergo blood test and willing to complete questionnaires and take medication as scheduled; and 4. Willing to provide written informed consent. Exclusion criteria 1. 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; 2. Patients receiving Chinese medicine in a regular pattern within the past 2 weeks; 3. Patients with chronic co-morbidities such as other fibrotic lung diseases in addition to pneumoconiosis and/or co-existing heart disease; 4. Patients with a medical history of malignancy within the past 5 years; 5. 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; 6. Patients with known severe cognitive and mental disorders; 7. Documented pregnancy or lactation; or 8. Patients allergic to the drug used in this study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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