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The Safety and Efficacy of Eucommia ulmoides Leaf Extract intervention for patients with hyperuricemia

The Safety and Efficacy of Eucommia ulmoides Leaf Extract intervention for patients with hyperuricemia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102376
Enrollment
Unknown
Registered
2025-05-13
Start date
2024-01-15
Completion date
Unknown
Last updated
2025-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperuricemia

Interventions

Placebo control group:The volunteers in this group were given dietary guidance, limiting the intake of high-purine foods such as animal organs, beer and sugary drinks, maintaining three regular meals
Low-dose Eucommia ulmoides leaf extract intervention group:The volunteers in this group were given dietary guidance, limiting the intake of high-purine foods such as animal organs, beer and sugary dri
High-dose Eucommia ulmoides leaf extract intervention group:The volunteers in this group were given dietary guidance, limiting the intake of high-purine foods such as animal organs, beer and sugary dr

Sponsors

College of Public Health, Medical College, Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: According to the 2019 edition of the Chinese Guidelines for the Diagnosis and Treatment of Hyperuricemia and Gout, regardless of gender, if an adult's fasting blood uric acid level exceeds 420 µ mol/L on a daily diet, it can be diagnosed as hyperuricemia (HUA). 1. Meet the above diagnostic criteria for HUA in Western medicine, with 420 µ mol/L<SUA; 2. The patient is aged between 18 and 65 years old; 3. Have not taken any other traditional Chinese medicine in the past 6 months; 4. Failure to participate in clinical research, or cessation of drug elution for more than 6 months after participating in clinical research; 5. Voluntarily sign an informed consent form and cooperate with the treatment provider.

Exclusion criteria

Exclusion criteria: 1. Those who do not meet the above diagnostic criteria and inclusion criteria; 2. Secondary HUA caused by malignant tumor, kidney disease, diabetes or other diseases and treatment methods; 3. During the acute gouty arthritis attack period, there are symptoms of joint redness, swelling, heat, and pain; 4. Those who use drugs such as salicylates, furosemide, and thiazide that affect SUA metabolism; 5. Those who plan to undergo surgery in the near future; 6. Individuals with severe cardiovascular disease; 7. Patients with severe kidney damage (ClScr<30ml/min) and/or severe liver damage (Child Pugh C grade); 8. Use of psychoactive substances, drug abuse and dependence; 9. Individuals with a recent history of excessive drinking or alcoholism; 10. Individuals who have experienced allergies to the intervention components used in this study; 11. Those who have not taken the intervention according to regulations, cannot judge the efficacy, or have incomplete data that affects the efficacy or safety judgment.

Design outcomes

Primary

MeasureTime frame
Uric acid, UA;

Secondary

MeasureTime frame
Fasting blood glucose, FBG;Total cholesterol, TC;Triglycerides, TG;Low-density lipoprotein, LDL;High-density lipoprotein, HDL;Body mass index, BMI ;CRP;

Countries

China

Contacts

Public ContactHui Liang

College of Public Health, Medical College, Qingdao University

qdlianghui@126.com+86 186 1532 9686

Outcome results

None listed

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