← Eichor
Study identifier: NCT02726555 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

The Efficacy and Safety of Combined Therapy With Red Yeast Rice and Low-dose Statin:Comparing With Standardized Statin

Condition: Dyslipidemia · Atherosclerosis  ·  Sponsor: Wenzhou Medical University

PhasePhase 3
Planned participants240
Who can joinAll sexes, 20 Years to 80 Years
Healthy volunteersNo

About this study

Double-dose statin regimen achieves merely 6% of decrease in low-density lipoprotein cholesterol (LDL-C) levels, whereas the risk of side effects increased largely. The investigators' previous pilot study (NCT01686451) has suggested that red yeast rice was of similar lipid-lowering efficacy while was associated with less fatigue than statins. The purpose of this study is to evaluate the efficacy and safety of combined therapy with red yeast rice and low-dose atorvastatin in persons with mild atherosclerotic cardiovascular disease and who qualified for statin therapy according to national guidelines.

This description comes directly from the study's public registry record.

Talk to the study team

Kangting Ji, MD  ·  +8613676403180  ·  jikt@wzmc.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

The Second Hispital of Wenzhou Medical UniversityWenzhou, Zhejiang, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT02726555