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 @ 4:58 PM
Ignite Modification Date:
2025-12-24 @ 4:58 PM
NCT ID:
NCT02340650
Eligibility Criteria:
Inclusion Criteria:
* Diagnosed with clinically suspicious bladder lesion or clinical finding; or who are undergoing cystoscopy as part of their routine clinical care.
* Must be willing and able to participate and provide written informed consent
* Women of childbearing age who have the possibility of being pregnant must have a negative pregnancy test prior to participation
Exclusion Criteria:
* Patient with sufficient evidence of cognitive impairment that limits the subject's ability to understand the protocol, provide informed consent, or to comply with the protocol procedures.
* Women with the possibility of having the pregnancy.
* Patients having acute infection.
* Person with Lidocaine sensitivity.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02340650
Study Brief:
Protocol Section:
NCT02340650