Skip to content

Effect of hypercholesterolemia alone or combined with hypertension on the degree of coronary artery stenosis in patients with coronary heart disease angina pectoris: a medical records based retrospective study

Effect of hypercholesterolemia alone or combined with hypertension on the degree of coronary artery stenosis in patients with coronary heart disease angina pectoris: a medical records based retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033863
Enrollment
Unknown
Registered
2020-06-14
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Coronary heart disease angina pectoris

Interventions

Case series:Nil

Sponsors

Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged between 35-75 years old; 2. Patients admitted from September 1, 2014 to September 1, 2019; 3. Patients with coronary heart disease and angina pectoris who underwent coronary angiography in the inpatient department of cardiovascular medicine; 4. The diagnosis of coronary heart disease, angina pectoris, hypercholesterolemia and hypertension in the inpatient department of Cardiology met the diagnostic criteria.

Exclusion criteria

Exclusion criteria: 1. Patients with other heart diseases, neurosis, climacteric syndrome, hyperthyroidism, cervical spondylosis of spinal cord or vertebral artery type, gastroesophageal reflux disease or esophageal hiatal hernia that may cause chest pain; 2. Patients with acute myocardial infarction, third degree of heart failure, myocarditis, cardiomyopathy, severe heart valve disease, infectious or systemic inflammatory diseases; patients with major diseases such as liver failure or renal failure, malignant tumor and serious metabolic diseases; 3. Pregnant women, lactating women or women of childbearing age with childbearing requirements; 4. Patients with psychosis or cognitive impairment; 5. Patients with iodine contrast agent allergy; 6. The researcher thinks there are other circumstances that are not suitable for participating in the study.

Design outcomes

Primary

MeasureTime frame
Clinical biochemical tests such as FPG, HbA1c, TC, TG, LDL-C, HDL-C, CRP, Fib and other indicators;CAG data in imaging examination;

Countries

China

Contacts

Public ContactChunquan Yu

Tianjin University of Traditional Chinese Medicine

ycq-4@163.com+86 18622569428

Outcome results

None listed

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