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 @ 11:33 PM
Ignite Modification Date:
2025-12-24 @ 11:33 PM
NCT ID:
NCT04960956
Eligibility Criteria:
Inclusion Criteria:
1. Males ≥ 18 years old at the time of informed consent
2. Ability to provide written informed consent and HIPAA authorization
3. Willingness to donate a fasting urine sample for research Patient Cohort
1. Histologically confirmed prostate or urothelial carcinoma
2. Localized disease
3. No neoadjuvant chemotherapy for disease Healthy Volunteer Cohort
<!-- -->
1. Healthy volunteers must not have prostate or urothelial carcinoma
Exclusion Criteria:
1. Concurrent disease or condition that would make the subject inappropriate for study participation or any serious medical or psychiatric disorder that would interfere with the subject's safety
2. Dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
18 Years
Study:
NCT04960956
Study Brief:
Protocol Section:
NCT04960956