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 @ 11:36 PM
Ignite Modification Date:
2025-12-24 @ 11:36 PM
NCT ID:
NCT04615156
Eligibility Criteria:
Inclusion Criteria:
* Known or suspected disease for which 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography Computed Tomography is appropriate for the investigation of. This includes, but is not limited to: Known or suspected cancer, neurological disorders (dementia or epilepsy), cardiac conditions (inflammation or myocardial viability), known or suspected presence of infection/inflammation process
Patients must satisfy all the following:
* Able to provide written informed consent, or consent obtained from appropriate guardian
* Able to tolerate the physical and logistic requirements of completing a Positron Emission Tomography Computed Tomography scan
Exclusion Criteria:
* Pregnant women: if there is any possibility of pregnancy, a blood Beta Human Chorionic Gonadotropin level will be obtained as per Eastern Health policy.
* Patients unwilling or unable to stop breast feeding for 12 hours
* Patients who are too medically unstable to tolerate the uptake period or lie flat for the duration of the scan
* Patients who exceed the safe weight limit of the Positron Emission Tomography Computed Tomography scanner bed (500 lbs.) or who cannot fit through the bore (70 cm diameter)
* Patients unwilling to proceed with scan (I.e. claustrophobia) prior to injection
* If patients inability to follow staff direction causes a safety hazard prior to injection
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT04615156
Study Brief:
Protocol Section:
NCT04615156