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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05105321
Other study ID # CSCF2021A04
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date December 2021
Est. completion date December 2028

Study information

Verified date November 2021
Source Peking University Third Hospital
Contact Wenyao Wang, MD, PhD
Phone 0086-18810488381
Email wwypumc@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The metabolic syndrome population is at high-risk of cardiovascular diseases and diabetes. How to effectively control the risk factors of this population is the key to primary prevention of cardiovascular diseases and diabetes in China. This study aims to explore the efficacy and safety of an intervention strategy with berberine that can effectively treat a variety of risk factors (hyperglycemia, dyslipidemia, hypertension).


Description:

Metabolic syndrome (MS) is a condition with multiple abnormal metabolic components, including obesity, dysglycemia, dyslipidemia and hypertension. The components of metabolic syndrome are major risk factors for cardiovascular disease and diabetes. Cardiovascular disease (CVD) is the primary cause of death and disease burden in China. This study aims to explore an intervention drug that can effectively control a variety of risk factors (hyperglycemia, dyslipidemia, hypertension), so as to improve the effectiveness and practical feasibility of primary prevention. Berberine is a drug with multiple function. Basic studies and previous clinical studies suggest that it has definite regulatory effects on blood glucose, lipid levels and blood pressure with few adverse reactions. This study selected pleiotropic Berberine as a means of intervention. It would provide new thought and high-level evidence for the primary prevention of cardiovascular disease and diabetes in Chinese population.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 5200
Est. completion date December 2028
Est. primary completion date December 2026
Accepts healthy volunteers No
Gender All
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria: - Patients diagnosed with metabolic syndrome aged 40-75 years old. - Metabolic syndrome was defined according to the Chinese Guidelines for the Prevention and Treatment of Dyslipidemia in Adults (revised edition 2016). Subjects will be diagnosed with metabolic syndrome when meeting three or more of the following items: 1, central obesity and/or abdominal obesity (waist circumference =90cm for men and = 85cm for women); 2, hyperglycemia (fasting blood glucose =6.10 mmol/L or two-hour blood glucose =7.80 mmol/L in glucose tolerance test); 3, hypertension: blood pressure =130/85 mmHg and/or diagnosed hypertension under treatment; 4, fasting triglyceride =1.7 mmol/L (150mg/dl); 5, fasting HDL cholesterol<1.0 mmol/L. Exclusion Criteria: - Previously diagnosed diabetes. - Baseline LDL cholesterol=130mg/dl (3.4mmol/L). - Baseline triglyceride=500mg/dl (5.6mmol/L). - Baseline blood pressure =140/90 mmHg (twice not on the same day). - Impaired liver function, have obvious clinical signs or symptoms of liver disease, acute or chronic hepatitis, alanine/aspartate aminotransferase levels >3 times the upper limit of the reference range at the screening visit. - Renal dysfunction (glomerular filtration rate<45ml/min) - Patients ventilated by ventilator. - Hypersensitivity to berberine. - Disease which may cause tissue hypoxia (especially acute disease, or worsening of chronic respiratory disease). - Severe chronic gastrointestinal disease. - Severe psychiatric illness. - Cancer requiring treatment in past 5 years. - Women who are pregnant or breastfeeding . - Participation in another clinical trial within the past 30 days . - Other significant disease that in the Investigator's opinion would exclude the subject from the trial.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Berberine
The tablet of berberine and placebo are both coated with white sugar and had the same appearance. Berberine tablet will be orally taken with a dose of 500mg twice daily
Behavioral:
Healthy lifestyle intervention
Healthy lifestyle intervention will be launched according to the "Chinese guidelines on prevention of cardiovascular and metabolic diseases by Chinese Preventive Medical Association in 2019", including health lectures, health information promotion, health manual and so on.

Locations

Country Name City State
China Peking University Third Hospital Beijing Beijing

Sponsors (2)

Lead Sponsor Collaborator
Tang Yida Chinese Society of Cardiology

Country where clinical trial is conducted

China, 

References & Publications (3)

Arnett DK, Blumenthal RS, Albert MA, Buroker AB, Goldberger ZD, Hahn EJ, Himmelfarb CD, Khera A, Lloyd-Jones D, McEvoy JW, Michos ED, Miedema MD, Muñoz D, Smith SC Jr, Virani SS, Williams KA Sr, Yeboah J, Ziaeian B. 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J Am Coll Cardiol. 2019 Sep 10;74(10):1376-1414. doi: 10.1016/j.jacc.2019.03.009. Epub 2019 Mar 17. Erratum in: J Am Coll Cardiol. 2019 Sep 10;74(10):1428-1429. J Am Coll Cardiol. 2020 Feb 25;75(7):840. — View Citation

Chang W, Chen L, Hatch GM. Berberine as a therapy for type 2 diabetes and its complications: From mechanism of action to clinical studies. Biochem Cell Biol. 2015 Oct;93(5):479-86. doi: 10.1139/bcb-2014-0107. Epub 2014 Dec 1. Review. — View Citation

Kong W, Wei J, Abidi P, Lin M, Inaba S, Li C, Wang Y, Wang Z, Si S, Pan H, Wang S, Wu J, Wang Y, Li Z, Liu J, Jiang JD. Berberine is a novel cholesterol-lowering drug working through a unique mechanism distinct from statins. Nat Med. 2004 Dec;10(12):1344-51. Epub 2004 Nov 7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of composite cardiometabolic endpoints The composite endpoints including cardiac death, nonfatal myocardial infarction, nonfatal stroke, and newly-diagnosed type 2 diabetes. three year
Secondary Rate of composite endpoints of cardiovascular diseases 1 The composite endpoints including cardiac death, nonfatal myocardial infarction, nonfatal stroke. three year
Secondary Rate of composite end point of cardiovascular disease 2 The composite endpoints including cardiac death, nonfatal myocardial infarction, nonfatal stroke, successful resuscitation of cardiac arrest, heart failure, arterial revascularization. three year
Secondary Rates of each component of the composite end point Each component of the composite end point three year
Secondary Rate of all-cause mortality Death due to all causes. three year
Secondary Rate of newly diagnosed prediabetes Prediabetes including impaired fasting glucose and abnormal glucose tolerance. three year
Secondary Rate of newly diagnosed hypertension Hypertension is defined as blood pressure=140/90 millimeters of mercury measured twice at not same day. three year
Secondary Rate of newly diagnosed malignancy Newly diagnosed malignancy. three year
Secondary Concentrations of serum lipid parameters Serum lipid parameters including total cholesterol, LDL cholesterol, HDL cholesterol, non-HDL cholesterol, triglycerides, Lp(a). three year
Secondary Changes of abdominal circumference Measurement of abdominal circumference in centimeter three year
Secondary Changes of waist-hip ratio Measurement of waist-hip ratio three year
Secondary Changes of body mass index Measurement of body mass index in kg/m^2 three year
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