Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:14 PM
Ignite Modification Date:
2025-12-24 @ 11:14 PM
NCT ID:
NCT05361356
Eligibility Criteria:
Inclusion Criteria:
* Volunteers (ages 18 to 75);
* Negative pregnancy tests for women of childbearing age;
* Agree to participate in the clinical trial and sign the subject informed consent form;
* Enhanced scan requires laboratory evidence of normal renal function.
Exclusion Criteria:
* The body cannot comply with CT examination;
* Pregnant and lactating women;
* Claustrophobia;
* People who are not suitable for enhanced scanning with iodine contrast agent (previous severe heart failure and hyperthyroidism, iodine contrast agent allergy and susceptibility);
* Patients deemed unsuitable for participation in this clinical trial by the investigator.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT05361356
Study Brief:
Protocol Section:
NCT05361356