Skip to content

The effect and mechanism of Pidotimod on hyperlipidemia induced arterial stiffness

The effect and mechanism of Pidotimod on hyperlipidemia induced arterial stiffness

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ROC-16009365
Enrollment
Unknown
Registered
2016-10-18
Start date
2016-10-17
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

arterial stiffness

Interventions

Hyperlipemia group:atorvastatin
control group:none
Pidotimod in Hyperlipemia group:Pidotimod and atorvastatin
Placebo in Hyperlipemia group:Placebo and atorvastatin

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Hyperlipidemia: under normal diet, total cholesterol (TC) is more than or equal to 5.72mmo/L or triglyceride (TG) is more than or equal to 1.7mmol/L or low density lipoprotein (LDL-C) is more than or equal to 3.64mmol/L or high density lipid protein cholesterol (HDL-C) is less than or equal to 0.91mmol/L,twice within 2 weeks, at least one factor match and except for other causes of dyslipidemia. Inclusion of normal group aim to be the reference of arterial stiffness and inflammatory factors level.

Exclusion criteria

Exclusion criteria: 1. physical scars, hypersensitive constitution and gut allergies; 2. pregnant or lactating women; 3. except for patients with secondary obesity dyslipidemia: pituitary tumor, hypothalamic syndrome, thyroid and gonadal function. Withdrawal syndrome, Cushing's syndrome, polycystic ovary syndrome, water retention, obesity, etc.; 4. Tuberculosis disease, severe diabetes, cancer, cardiovascular and cerebrovascular disease patients; 5. Patients with bleeding tendency; 6. Local skin infection or ulcer patients; 7. Coronary heart disease and other heart disease 8. According to different research purposes and research drug prescribed population. In addition 1) are participating in other clinical trials of patients; 2) researchers believe other reasons are not suitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
pulse wave velovity;CRP;

Countries

China

Contacts

Public ContactBing Du

The first hospital of Jilin University

dbdavina@126.com+86 15804302181

Outcome results

None listed

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