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the efficacy and safety of chinese medicine granules in treatment of hyperlipidemia

Clinical study of Chinese medicine Granule in treatment of mild hyperlipidemia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003780
Enrollment
Unknown
Registered
2013-11-12
Start date
2013-12-01
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

treatment group:chinese herbs
control group:placebo

Sponsors

Baokang Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: age:18-75 years old;1.70 mmol/L (150mg/dl)< TG<4.52 mmol/L (399 mg/dl);LDL-C=3.37mmol/L;voluntarily signning informed consent.

Exclusion criteria

Exclusion criteria: Secondary dyslipidemia; Taking other drugs for treatment; Fast glucose =180mg/dl (10mmol/L), or HbA1C>8%; DBP>115mmHg?SBP>180mmHg; Active liver disease; ALT or/and AST was over the normal range 1.5 folds; Severe renal dysfunction (e.g.Creatinine clearance is less than the normal value of 25%); Combined with other serious primary diseases such as endocrine, hematopoietic system; Symptomatic cerebrovascular disease or new myocardial infarction in the past 3 months; Preparing fertility, pregnancy or lactation women in the future 3 months; Allergic constitution, or known allergic to any ingredient of the intervention; Taking part in other clinical trials.

Design outcomes

Primary

MeasureTime frame
serum lipid;Concentration of Br2+;medication adherence scal;

Secondary

MeasureTime frame
side effect;

Countries

China

Contacts

Public ContactZhang Junhua
zjhtcm@foxmail.com+86 022-59596173

Outcome results

None listed

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