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 @ 5:03 PM
Ignite Modification Date:
2025-12-24 @ 5:03 PM
NCT ID:
NCT03557450
Eligibility Criteria:
Inclusion Criteria:
Subjects must meet all of the following criteria to be included in the study.
1. 20 - 75 years old
2. Must be ambulatory and able to attend all appointments
3. Women must agree to use one of the following methods of birth control for the duration of the clinical trial:
systemic hormonal contraceptive (oral, injected, transdermal), intrauterine device, double barrier (e.g., cervical cap or diaphragm with condom or spermicide). Men with female partners must agree to use double barrier contraception, unless their partner is using systemic hormonal contraceptives or has an intrauterine device
4. Subject undergoing PET/CT scans must have the ability to lay motionless for up to 30 minutes.
Exclusion Criteria:
1. Subjects undergoing PET/CT scans must not be breast-feeding.
2. History of hypersensitivity to fluoride
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
20 Years
Maximum Age:
75 Years
Study:
NCT03557450
Study Brief:
Protocol Section:
NCT03557450