Ancient herbal recipe tested to save diabetic legs from ulcers
NCT ID NCT07658807
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether adding a traditional Chinese medicine formula called Bu Yang Huanwu Decoction (in capsule form) to standard treatment can prevent leg pain at rest or foot ulcers in people with diabetic lower extremity vascular disease. About 300 adults aged 18 to 70 with diabetes and early to moderate leg artery disease will be randomly assigned to receive either standard care plus the herbal capsules or standard care alone for 6 months. The main goal is to see if the herbal formula reduces the chance of developing serious leg complications over one year.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Hua Yu Wan Capsule (a modern preparation of the traditional Chinese medicine formula Bu Yang Huanwu Decoction)
- What this could lead to
- If it works, this could point toward a new way to prevent serious leg complications in people with diabetes, potentially reducing the need for amputation.
- What could go wrong
- This is a single Phase 3 trial with 300 participants, so results may not apply to everyone. The herbal formula may not provide additional benefit over standard care, 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 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2029
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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18 to 70 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.
Show the full entry requirements Hide the full entry requirements
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 18 to 70 years (inclusive), male or female. 2. Diagnosed with diabetes mellitus according to the Chinese Diabetes Society (2024) Guidelines. 3. Glycated hemoglobin (HbA1c) \< 12%, with recent fasting blood glucose \< 7.0 mmol/L OR postprandial blood glucose \< 10.0 mmol/L, and triglycerides \< 1.7 mmol/L. 4. Diagnosed with LEAD, meeting the following criteria: Rutherford Classification 2, 3, or 4. Resting ABI ≤ 0.90, OR for patients with exertional symptoms and resting ABI \> 0.90, a post-exercise treadmill test showing an ABI decrease of ≥15%. Evidence of lower limb arterial stenosis or occlusion confirmed by duplex ultrasound, CTA, MRA, or DSA. 5. TCM Pattern Diagnosis: Must conform to the TCM syndrome of Qi Deficiency and Blood Stasis, as defined by the study's TCM diagnostic criteria (referencing "Practical Diagnostic Criteria for Blood Stasis Syndrome" and "Integrated Chinese and Western Medicine Peripheral Vascular Disease"): Main Symptom: Lower limb weakness, or feeling of heaviness/discomfort after prolonged walking. Secondary Symptoms: Shortness of breath/lassitude in speaking; dry mouth with desire to drink; scaly skin. Tongue \& Pulse: Tongue with teeth marks, pale-purple with petechiae/ecchymosis; thin and choppy pulse. (Diagnosis confirmed by meeting 1 main symptom OR 2 secondary symptoms, assessed by a qualified TCM practitioner.) 6. Voluntarily signs the Informed Consent Form (ICF) and is willing and able to comply with all study procedures and visits. Exclusion Criteria: 1. Known bleeding disorders or history of intracranial hemorrhage. 2. Current use of anticoagulants (e.g., warfarin, dabigatran, factor Xa inhibitors). 3. Presence of active infection. 4. Severe cardiac abnormalities on resting ECG (e.g., heart failure, ventricular tachycardia, ventricular fibrillation, multifocal ventricular contractions, prolonged corrected QT interval). 5. History of acute coronary syndrome ≤ 12 months requiring dual antiplatelet therapy. 6. Chronic liver disease (Child-Turcote-Pugh score ≥5) or chronic kidney disease stages 4-5 (eGFR \< 30 mL/min/1.73m²). 7. History of malignancy (except cured basal cell carcinoma). 8. Moderate to severe anemia, polycythemia vera, or any hyperviscosity syndrome. 9. Planned lower limb revascularization or amputation. 10. Concurrent or planned use of medicinal products containing Veratrum species. 11. Pregnant or lactating women, or women of childbearing potential not using highly effective contraception. 12. Known allergy or hypersensitivity to any component of the study medication (Qilong Capsules, aspirin). 13. Patients with psychiatric disorders or judged to be uncooperative. 14. Currently participating in another drug clinical trial or using therapies with similar purported effects. 15. Any other condition deemed by the investigator to make the participant unsuitable for the trial.
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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 places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Xuanwu Hospital
Beijing, China
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