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Clinical study on the treatment of qi stagnation and phlegm obstruction dyslipidemia with Jieyu Qutan Huazhuo prescription

Clinical study on the treatment of qi stagnation and phlegm obstruction dyslipidemia with Jieyu Qutan Huazhuo prescription

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005539
Enrollment
Unknown
Registered
2022-01-15
Start date
2022-01-23
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

hypertriglyceridemia

Interventions

Control group:Jieyu Qutan Huazhuo prescription placebo
Experimental group:Jieyu Qutan Huazhuo prescription

Sponsors

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

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Aged between 18 and 80; (2) Meet the diagnostic criteria of hypertriglyceridemia; (3) Meet the diagnostic criteria of qi stagnation and phlegm obstruction syndrome; (4) Those who are using other lipid-lowering drugs or therapies (including physical therapy) should stop taking the drugs or stop the therapy and still meet the above standards after 2 weeks of elution; (5) Voluntarily join the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Secondary hypertriglyceridemia caused by hypothyroidism, nephrotic syndrome, diabetes and other diseases; (2) Have suffered from acute cardiovascular and cerebrovascular events or severe trauma within 1 year; (3) Patients who need to take drugs with definite influence on triglyceride level for a long time after previous PCI or other major surgery; (4) Patients suffering from systemic serious diseases of the heart, brain, liver, kidney and immune system, or mental patients; (5) The patient is using drugs that affect lipid metabolism, such as glucocorticoids, thyroid hormones, and moderate potency diuretics (6) The patient or his/her spouse is in the stage of pregnancy, pregnancy or lactation; (7) People who may be allergic to the drug in this test; (8) Other circumstances that may affect the efficacy and safety of the test drug.

Design outcomes

Secondary

MeasureTime frame
TCM syndrome score;

Primary

MeasureTime frame
Triglyceride levels;

Countries

China

Contacts

Public ContactKuiwu Yao
yaokuiwu@126.com18610366611

Outcome results

None listed

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