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Clinical evaluation of Jiang Zhi Qing Shen Capsules in the treatment of hyperlipidemia (phlegm and turbidity blocking type)

Clinical evaluation of Jiang Zhi Qing Shen Capsules in the treatment of hyperlipidemia (phlegm and turbidity blocking type)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071936
Enrollment
Unknown
Registered
2023-05-30
Start date
2023-05-30
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Dyslipidemia

Interventions

Test group:Rosuvastatin + Jiang Zhi Qing Shen Capsules
Control group:Rosuvastatin + placebo

Sponsors

Zhengzhou Chinese Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Meeting the diagnostic criteria of primary dyslipidemia in Western medicine; (2) Meet the diagnostic criteria of the Chinese medical evidence (phlegm and turbidity blocking type); (3) Between the ages of 18 and 70 years old, with independent ability, regardless of gender; (4) have taken lipid-lowering drugs, but have stopped taking them for 15 days or more, and the lipid level has not reached the standard, but still meets the current diagnostic criteria (4) have taken lipid-lowering drugs, but have stopped taking them for 15 days or more, and the blood lipid level has not reached the standard, but still meets the current diagnosis criteria (5) Voluntary participation in the clinical trial, and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) Secondary dyslipidemia: dyslipidemia disorders caused by long-term or high-dose medication, or dyslipidemia caused by endocrine diseases, liver and kidney diseases, etc. (1) Secondary dyslipidemia: dyslipidemia caused by long-term, high-dose medication, or dyslipidemia caused by endocrine diseases, liver and kidney diseases, etc; (2) Pregnant or lactating women, or women who are preparing for pregnancy; (3) Patients who are allergic to HMG-CoA reductase inhibitors; (4) Diseases related to weight change such as diabetes, peptic ulcer or malabsorption syndrome; (5) Familial dyslipidemia with a genetic predisposition due to genetic abnormalities; (6) Patients with mental illness; (7) Patients with severe liver disease or renal insufficiency, severe cardiac insufficiency and other major cardiovascular events; (8) Other patients who, in the opinion of the investigator, are not suitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Total cholesterol;Triglycerides;Low-density lipoprotein cholesterol;High-density lipoprotein cholesterol;

Secondary

MeasureTime frame
Apolipoprotein A1;Apolipoprotein B;Lipoprotein (a);Fasting blood glucose;

Countries

China

Contacts

Public ContactLi Dongyu

Zhengzhou Chinese Hospital

18537199969@163.com+86 185 3719 9969

Outcome results

None listed

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