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 @ 12:31 AM
Ignite Modification Date:
2025-12-25 @ 12:31 AM
NCT ID:
NCT06708767
Eligibility Criteria:
Inclusion Criteria:
* Understands the requirements of the study and provides written informed consent prior to undergoing any study-related procedures
* Subject is between the ages of 18 to 85 years old, inclusive
* Has good venous access as determined by the Investigator at screening
* Weighs up to 450 lbs
Exclusion Criteria:
* Is pregnant (as determined by a urine pregnancy test at the time of consent)
* Has significant cardiovascular, respiratory, hepatic, gastrointestinal, hematological, neurological, psychiatric or other disease that may interfere with the objectives of the study and/or pose safety concerns;
* Has evidence of moderate to severe renal insufficiency or renal failure (defined as an estimated glomerular filtration rate \<60 ml/minute)
* Has an allergy to iodinated or other medical intravenous contrast material
* Weighs more than 450 pounds
* Is breastfeeding
* Is a woman of childbearing age who is not using double protection birth control
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
85 Years
Study:
NCT06708767
Study Brief:
Protocol Section:
NCT06708767