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 @ 4:40 PM
Ignite Modification Date:
2025-12-24 @ 4:40 PM
NCT ID:
NCT02443766
Eligibility Criteria:
Inclusion Criteria:
* Able to give informed consent and willing to complete the study.
* Willing to undergo the full imaging procedures.
* Women of childbearing potential with a negative serum pregnancy test.
Exclusion Criteria:
* Any neurological or psychiatric disorders, including drug or alcohol abuse, that may interfere with cerebral blood flow as determined by the principal investigator.
* Any medical conditions that may interfere with cerebral blood flow as determined by the principal investigator.
* Currently taking medication that might affect cerebral blood flow (i.e. antidepressants, antipsychotics, anxiolytics, benzodiazepines, sedatives, antiseizure medications)
* Subject is unable or unwilling to lie still in the scanner (i.e. due to claustrophobia or weight \> 350 pounds)
* Subject has metal in their body or other reason that they cannot undergo magnetic resonance imaging.
* Previous brain surgery or intracranial abnormalities they may complicate interpretation of the brain scans. (e.g. stroke, tumor, vascular abnormality).
* Pregnancy
* Allergy to iodine or shellfish.
* Concurrent participation in another research protocol that might affect the outcome of this study as determined by the principle Investigator.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02443766
Study Brief:
Protocol Section:
NCT02443766