chronic coronary syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria for patients with chronic coronary syndrome: (1) Meet any of the diagnostic criteria in the Diagnosis and Guidelines for Chronic Coronary Syndromes; (2) Have a history of angina pectoris attacks for 3 months or more no less than 2 attacks per week and the frequency degree and remission time of each attack are stable or there are no angina symptoms and there are chest tightness and palpitation; (3) Those who have been screened with typical acupoint sensitization characteristics; (4) 18= age=85 gender is not limited; (5) Those who are willing to participate in the trial and sign the informed consent form. Inclusion criteria for healthy subjects (1) 18= age=85 gender is not limited; (2)No history of chronic coronary syndrome or other heart diseases; (3) Those who are willing to participate in the trial and sign the informed consent form.
Exclusion criteria
Exclusion criteria: Exclusion criteria for patients with chronic coronary syndrome: (1) Patients with acute coronary syndrome (acute myocardial infarction unstable angina) severe arrhythmia (severe atrioventricular block ventricular tachycardia frequent premature ventricular contractions atrial fibrillation) severe heart failure (heart failure rated as NYHA grade III or IV) severe valvular heart disease primary cardiomyopathy dissecting aneurysm pulmonary embolism stroke accompanied by severe liver and kidney dysfunction; (2) Those with coagulation disorders bleeding risk or scar constitution blood diseases (leukemia hemophilia hepatitis B AIDS etc.); (3) Those who have skin ulceration or skin diseases at the sensitized site; (4) Pregnant and lactating women patients with mental diseases; (5) Those who participate in other clinical research at the same time. Exclusion criteria for healthy subjects (1) Those with coagulation disorders bleeding risk or scar constitution blood diseases (leukemia hemophilia hepatitis B AIDS etc.); (2)Those who have skin ulceration or skin diseases at the Sampling site; (3) Pregnant and lactating women patients with mental diseases; (4) Those who participate in other clinical research at the same time.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nav1.7;5-HT;TRPV1;CGRP; | — |
Countries
China
Contacts
Shaanxi University of Traditional Chinese Medicine