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Ancient herbal recipe tested to save diabetic legs from ulcers

NCT ID NCT07658807

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

Phase 3

Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.

Participants

About 300 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Jan 2029

An estimate. End dates often move.

Lead sponsor

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

18 to 70 years

Sex

Anyone

Healthy volunteers

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

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

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  1. The places running it

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  2. The official record

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  3. A doctor treating you

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Contacts and locations

Locations

  • Xuanwu Hospital

    Beijing, China

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Other studies related to the condition(s) this trial covers.