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A randomized controlled clinical study on noninferiority of Feng's steam therapy in the treatment of dyslipidemia

A randomized controlled clinical study of Feng's steam therapy in the treatment of dyslipidemia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038005
Enrollment
Unknown
Registered
2020-09-08
Start date
2020-09-14
Completion date
Unknown
Last updated
2020-11-16

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

Conditions

Dyslipidemia

Interventions

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria of Western medicine for hypercholesterolemia or mixed hyperlipidemia; (2) TCM differentiation is the syndrome of damp turbid arthralgia; (3) Aged over 18 and under 75 years; (4) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients who have suffered from acute myocardial infarction, cerebrovascular accident, severe trauma, post-PCI or other major surgery within six months and need to take lipid-lowering drugs for a long time; (2) Patients with acute coronary syndrome; (3) Those with secondary hyperlipidemia caused by nephrotic syndrome, hypothyroidism, gout, acute or chronic hepatobiliary disease, diabetes, etc.; (4) Hyperlipidemia caused by drugs (phenothiazines, ß-receptor blockers, adrenal corticosteroids, and certain contraceptives, etc.) or who are using heparin, thyroxine therapy drugs and other drugs that affect blood lipid metabolism patient; (5) Combined with serious primary diseases such as liver, kidney and hematopoietic system; (6) Pregnant or lactating women or those who plan to become pregnant during the trial period or whose spouse plans to become pregnant; (7) Those who are allergic or may be allergic to this treatment; (8) Patients with heart failure and heart function >= NYHA III; combined with severe arrhythmia (such as frequent ventricular premature, ventricular tachycardia, rapid atrial fibrillation, etc.) or other severe or unstable heart, liver, kidney, endocrine, Patients with medical diseases such as blood; (9) Patients with uncontrolled grade 3 hypertension (sitting diastolic blood pressure >= 110mmHg or systolic blood pressure >= 180mmHg; (10) People with mental illness, alcohol or drug dependence; (11) Patients with liver and kidney damage, ALT >= 1.5N, Cr > 1N (N is the upper limit of normal); (12) Those with a history of malignant tumors or related diseases; (13) Subjects participated in other clinical trials within 1 month; (14) People with infectious skin diseases or skin injuries; (15) Any other situation that the investigator believes will affect the efficacy and safety of the trial drug treatment.

Design outcomes

Primary

MeasureTime frame
Total cholesterol;Triglycerides;LDL cholesterol;High density lipoprotein cholesterol;

Countries

China

Contacts

Public ContactFeng Ling

Guang'anmen Hospital Affiliated to China Academy of Chinese Medical Sciences

flyutong@163.com+86 13401067188

Outcome results

None listed

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