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:
2025-12-25 @ 2:22 AM
Ignite Modification Date:
2025-12-25 @ 2:22 AM
NCT ID:
NCT03878134
Eligibility Criteria:
* INCLUSION CRITERIA:
* NIH patients currently on an NIH research protocol who are referred to RAD\&IS for CT examination as part of that research protocol
* 18 years old or greater
* Able to understand and sign informed consent
EXCLUSION CRITERIA:
* Studies that specifically require simultaneous dual source CT scan capability or where dual source CT scan is requested
* Studies ordered for an emergency indication
* Pregnant women. Subjects of child-bearing potential will undergo serum or urine pregnancy testing within 72 hours before examination. Post-menopausal and surgically sterilized subjects are automatically exempt from this testing
* Lactating women who are unable to stop breast feeding for 24 hours following the administration of contrast
* Body weight \>500 lbs (227 kg) or a body circumference that prevents the study subject from lying flat in the scanner
* Patients who have undergone PCCT examination within the past year.
* Any contraindications that the research team identifies from the subject, RAD\&IS CT questionnaires, and/or History and Assessment
* Employees or staff supervised by the Principal Investigator or an Associate will not be recruited to participate
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03878134
Study Brief:
Protocol Section:
NCT03878134