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A random clinical trial study to assess the efficiency of fumigation with Lishi-jiangzhi Decoction in the treatment of hyperlipoidemia

A random clinical trial study to assess the efficiency of fumigation with Lishi-jiangzhi Decoction in the treatment of hyperlipoidemia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14005130
Enrollment
Unknown
Registered
2014-08-13
Start date
2014-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Hyperlipidemia

Interventions

Simvastatin treatment group:Simvastatin
placebo:Fumigation with placebo
Fumigation with LSJZ:Fumigation with Lishi Jiangzhi (reducing lipids) decoction

Sponsors

Guanganmen Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Male or female who meets research diagnostic criteria for hyperlipidemia: TC more than 6.22 mmol/L or TG more than 2.26 mmol/L or LDL-C more than 4.14mmol/L or HDL-C less than 1.04 mmol/L; 2. Being up to diagnostic criteria of phlegm-damp and blood stasis syndrome in TCM; 3. Range in age from 30 to 70; 4. Voluntarily signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. The patient has suffered acute myocardial infarction, cerebral vascular accident, severe trauma or big reforms within six months. Or the patient who has high blood pressure don't have it under control(higher than 180/110 mmHg); 2. Hyperlipidemia due to nephritic syndrome, hypothyroidism, gout, acute or chronic hepatobiliary diseases, diabetes and so on; 3. Hyperlipidemia is caused by the use of drugs, familial hypercholesterolemia and TG more than 11.3 mmol/L; 4. The patient is using heparin, thyroid hormone or other drugs which can cause metabolic disorder of serum lipids. Or the patient is using other lipid-lowering agents within 2 weeks; 5. The patient has severe vital primary disease of liver, kidney, hematopoietic system and other systems, or a psychopath.

Design outcomes

Primary

MeasureTime frame
Cholesterol;Triglycerides;Low-density lipoprotein;High-density lipoprotein;

Secondary

MeasureTime frame
Weight;TCM symptoms;tongue picture;pulse;blood pressure;

Countries

China

Contacts

Public ContactLING FENG
flyutong@163.com+86 13401067188

Outcome results

None listed

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