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Analysis of sociological etiology of dyslipidemia and the interventional study of Jieyu Qutan Huazhuo Prescription

Analysis of sociological etiology of dyslipidemia and the interventional study of Jieyu Qutan Huazhuo Prescription

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016794
Enrollment
Unknown
Registered
2018-06-25
Start date
2018-06-15
Completion date
Unknown
Last updated
2018-11-05

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

Conditions

Dyslipidemia

Interventions

Group 1:jieyuqutanhuazhuo prescription
Group 2:Xuezhikang capsule

Sponsors

Guang'anmen Hospital China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the Western medical diagnostic criteria for dyslipidemia:TC=6.22mmol/L or TG=2.26mmol/L or LDL-C=4.14mmol/L or HDL-C<1.04mmol/L; 2. Patients aged 18-80 years; 3. Fulfill diagnostic criteria for the TCM syndrome of qi depression and phlegm obstruction. 4. Voluntarily joined this study and has signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Have suffered from acute myocardial infarction, cerebrovascular accident, severe trauma, etc. within half a year; 2. Secondary dyslipidemia caused by diseases such as hypothyroidism, nephrotic syndrome, diabetes, etc. 3. Patients who need long-term use of lipid-lowering agents after PCI or other major surgery. 4. Drugs that affect blood lipid metabolism or thyroid treatment drugs such as glucocorticoids, thyroid hormones, thiazide diuretics, and beta blockers are being used. 5. Patients with systemic serious diseases such as heart, liver, kidney, hematopoietic system, and immune system. 6. Pregnant, lactating women or who plan to become pregnant during the trial or who plan to become pregnant. 7. Allergic constitution, patients who may be allergic to this drug or psychotic patient. 8. Any other situation that the investigators consider will affect the efficacy and safety of the investigational drugs.

Design outcomes

Primary

MeasureTime frame
TCM Symptom Scale;TC;TG;LDL-C;HDL-C;

Countries

China

Contacts

Public ContactYao Kuiwu

Guang'anmen Hospital China Academy of Chinese Medical Sciences

yaokuiwu@126.com+86 18610366611

Outcome results

None listed

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