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A Randomized Controlled Trial for Efficacy and Safety of berberine on vasculopathy in patients with NSTE-ACS after stenting

A Randomized Controlled Trial for Efficacy and Safety of berberine on vasculopathy in patients with NSTE-ACS after stenting

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018742
Enrollment
Unknown
Registered
2018-10-07
Start date
2018-10-15
Completion date
Unknown
Last updated
2018-10-15

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

Conditions

coronary atherosclerotic heart disease

Interventions

berberine group:The routine therapy with berberine 0.4g po t.i.d

Sponsors

The First Affiliated Hospital of Henan University of CM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Male or female aged 15 to 70 years old; 2. Consistent with NSTE-ACS diagnosis; 3. Patients who were confirmed to be suitable and successfully treated with PCI stents; 4. Patients agree with this clinical trail and sign the medical informed consent.

Exclusion criteria

Exclusion criteria: (1) STEMI,stable angina, aortic dissection, myocarditis, pericarditis, myocardiopathy, valvular disease; (2) Patients with pulmonary embolism, acute febrile and other inflammatory diseases and active infections, severe damage of liver or kidney (AST or ALT>3 times normal upper limit, TBIL>2 times normal upper limit), malignant tumors and hemorrhagic diseases; (3) Patients with Hemodynamic instability or serious complications after PCI; (4) Allergic to the experimental drug; (5) Patients in another clinical trial and take their research drugs; (6) Life expectancy was shorter than the duration of the study; (7) pregnant women; (8) favism; (9) Patients with any other conditions considered cannot be recruited.

Design outcomes

Primary

MeasureTime frame
coronary artery stenosis;adverse cardiovascular and cerebrovascular events within 12 months after PCI;

Secondary

MeasureTime frame
fasting blood glucose;Glycosylated hemoglobin;lipid metabolism;CRP;uric acid;homocysteine;blood pressure;Platelet inhibition ratio;PCSK9;PTX-3;

Countries

China

Contacts

Public ContactHuaimin Guan

The First Affiliated Hospital of Henan University of CM

guanhuaimin2004@aliyun.com+86 13603847890

Outcome results

None listed

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