None
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Age 18 to 75 years old; 2.Those who agree to participate in this clinical trial and sign the subject informed consent form; 3.Those who have full capacity for civil behavior.
Exclusion criteria
Exclusion criteria: 1.Persons who do not have full capacity for civil behavior; 2.Women during pregnancy and breastfeeding; 3.Persons at high risk of iodine contrast contraindication and allergy (only enhanced scan needs to be excluded); 4.Persons with renal insufficiency (to be excluded for enhanced scanning only); 5.Persons at high risk for contraindications and allergies to heart rate-lowering medications (excluded for coronary scans only). 6.Those who, in the opinion of the investigator, should not participate in this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical image quality acceptance rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Satisfaction with commonly used functions, ease of machine operation, overall machine functionality, and stability; | — |
Countries
China
Contacts
Zhongshan Hospital, Fudan University