Conventional lesion
Conditions
Interventions
Case series:None
Sponsors
Sun Yat-sen University Cancer Center
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. Aged between 18 and 75 years old. 2. For females, not pregnant or breastfeeding and using medicaally acceptable contraception. 3. Voluntary participation in this clinical trial and signing the informed consent form. 4. Individuals with full legal capacity.
Exclusion criteria
Exclusion criteria: 1. Individuals lacking full legal capacity. 2. Pregnant and lactating women. 3. Those with an intention for childbirth within the next 6 months. 4. Individuals with metallic implants. 5. High-risk individuals with contraindications or allergies to iodinaated contrast agents (only for contrast-enhanced scans). 6.Individuals with renal insufficiency, with glomerular filtration rate less than 90 milliters per minute (only for contrast-enhanced scans,and subjects must provide kidney function test results within one month; if unavailable, they must undergo kidney function assessment). 7.Individuals deemed unsuitable for participation in this clinical trial by the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Image validity; | — |
Secondary
| Measure | Time frame |
|---|---|
| ease of operation;safe reliability; | — |
Countries
China
Contacts
Public ContactMing Chen
Sun Yat-sen University Cancer Center
Outcome results
None listed