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Evaluation of the effect of Natto Hongqu Capsules on blood lipid regulation

Evaluation of the effect of Natto Hongqu Capsules on blood lipid regulation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064215
Enrollment
Unknown
Registered
2022-09-30
Start date
2022-09-30
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Dyslipidemia

Interventions

1:Simvastatin Placebo + Natto Hongqu Placebo
2:Simvastatin Placebo +Natto Hongqu Capsules
3:Simvastatin Tablet + Natto Hongqu Placebo
4:Simvastatin Tablet + Natto Hongqu Capsules

Sponsors

School of Public Health and Emergency Management, Southern University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 74 Years

Inclusion criteria

Inclusion criteria: 1. 35-74 years old; 2. High LDL-C population: meeting the criteria for marginally elevated LDL-C and dyslipidemia in the 2016 Chinese Guidelines for the Management of Dyslipidemia in Adults, that is, LDL-C level ranges from 3.4 mmol/L to 5.0 mmol/L after fasting for 10 hours, without definite causes or taking lipid-lowering medications; 3. The 10-year ASCVD risk calculated by the China-PAR prediction model derived from Chinese population is 5-10%.

Exclusion criteria

Exclusion criteria: 1. Patients with definitely diagnosed cardiovascular and cerebrovascular diseases (e.g., myocardial infarction, stroke, heart failure, valve heart diseases, arrhythmias), malignant tumors, secondary hyperlipidemia; or severe gastrointestinal diseases or surgery history; or severe liver disease (ALT and/or AST are more than three times the upper limit of normal); or severe kidney disease (stages 4 and 5 chronic kidney disease, or eGFR = 140/90 mmHg when prescribed >= 3 antihypertensive medications at optimal doses); or secondary hypertension; or BMI >= 30kg/m2; 3. Patients with familial hypercholesterolemia; or statin intolerance; or TG >= 5.6 mmol/L; 4. Patients taking aspirin, warfarin or other anticoagulants; or using corticosteroids, antiretroviral or antipsychotic medications; 5. Pregnant or lactating females; 6. Patients participating in other ongoing clinical trials; 7. Other circumstances not suitable for participation considered by researchers, such as planning to become pregnant or losing weight.

Design outcomes

Primary

MeasureTime frame
LDL-C;High Density Lipoprotein Cholesterol;Triglyceride;Total Cholesterol;

Secondary

MeasureTime frame
Systolic Blood Pressure;Diastolic Blood Pressure;Ankle-brachial Index;Blood Glucose;Heart Rate Variability;Carotid intima-media Thickness;Pulse Wave Velocity;Complete Blood Count;C-Reactive Protein;Arterial Velocity Pulse Index;Arterial Pressure Volume Index;Arterial Pressure Volume Index;

Countries

China

Contacts

Public ContactDongfeng Gu

Southern University of Science and Technology

gudf@sustech.edu.cn+86 13501386288

Outcome results

None listed

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