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Red Yeast Rice for Primary Prevention of Hypercholesterolemia

Gut Microbiota and Bile Acids Mediate the Clinical Benefits of Red Yeast Rice for Primary Prevention of Hypercholesterolemia: A Pilot Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06301906
Enrollment
41
Registered
2024-03-08
Start date
2024-02-26
Completion date
2025-12-31
Last updated
2026-03-20

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

Conditions

Hypercholesterolemia

Brief summary

This two-year observational study will be conducted at the outpatient clinic of the Department of Traditional Chinese Medicine of Taoyuan Chang Gung Hospital from February 26, 2024 to December 31, 2025. This study will enroll 35\ 55 year-old male patients who are expected to take LipoCol Forte Capsules for primary prevention of hypercholesterolemia. The investigators will collect the TCM constitution questionnaires from patients before taking LipoCol Forte Capsules and every three months after taking the medicine. At the same time, blood will be drawn to detect glycated hemoglobin, fasting blood sugar, insulin, lipids profile, liver and kidney function, creatine kinase, predictive parameters of atherosclerotic cardiovascular disease, and plasma bile acids, etc. Fecal samples will also be collected to analyze the intestinal microbiota and fecal bile acid composition. This study will evaluate the efficacy, durability and safety of LipoCol Forte capsules in the primary prevention of hypercholesterolemia in patients with different constitutions, as well as whether it can reduce the risk of cardiovascular disease, and its influence on bile acid metabolism and intestinal microbiota.

Interventions

DRUGLipoCol Forte Capsule 600mg twice a day

LipoCol Forte Capsule 600mg twice a day for 12 months

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
35 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Aged 35\~55 years old * LDL-C≥130mg/dl or patients with diabetes or chronic kidney disease with LDL-C ≥ 100mg/dl * expected to receive LipoCol Forte Capsule 600mg bid

Exclusion criteria

* Have received anti-hyperlipidemic drugs or red yeast rice treatment within the past month; * Female; * Have experienced rhabdomyolysis or abnormal liver function ALT \>72 U/L due to taking red yeast rice; * Bleeding diseases, such as abnormal platelets, abnormal coagulation factors, or gastrointestinal tract infection within one month * Liver insufficiency ALT \>72 U/L or renal insufficiency eGFR \< 30 mL/min/1.73 m2; * Have ever had coronary heart disease, myocardial infarction or cerebrovascular disease; * Stressful situations, including hospitalization or surgery within the past or next month, and cancer still being treated; * Uncontrolled hypertension (blood pressure ≥160/100 mmHg); * Use antibiotics, probiotics or weight-loss drugs for more than 3 consecutive days within 3 months before inclusion in the study; * Drug abuse or poor compliance; * Use of traditional Chinese medicine in the past month

Design outcomes

Primary

MeasureTime frameDescription
Low Density Lipoprotein-Cholesterol (LDL-C)before treatment, and 3, 6, 9, 12 months after treatmentsThis study will evaluate the efficacy and durability of LipoCol Forte capsules in the primary prevention of hypercholesterolemia.

Secondary

MeasureTime frameDescription
10-Year Atherosclerotic Cardiovascular Disease (ASCVD) Riskbefore treatment, and 3, 6, 9, 12 months after treatmentsuse ASCVD risk estimator to calculate the 10-Year ASCVD Risk after LipoCol Forte capsules treatment

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 21, 2026