Study Investigating Intravesical HDAC Inhibition to Improve Response to Immuno-Oncology Agents
NCT06963346
Bladder Cancer, Female Urogenital Diseases
Tampa, Florida, United States
View Trial DetailsNCT Number: NCT04503577
Prospective nation-wide cohort of high-risk non-muscle-invasive, muscle-invasive and metastatic bladder cancer in the Netherlands
Interested in participating?
Request Info18 year and older
All sexes
Observational
Jeroen Bosch Hospital, 's-Hertogenbosch, Netherlands
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Note: participation in ProBCI does not exclude the patient from participation in other studies.
Time frame: 10 years
Alive/death/emigrated
Time frame: 10 yeas
Progression/no progression
Time frame: 10 yeas
Recurrence/no recurrence
Time frame: 2 years
EQ-5D (EuroQol-Five Dimensions)
Time frame: 2 years
QLQ-C30 (Quality of Life Questionnaire-Cancer)
Contact information is provided by the study sponsor or research team.
Prospective Bladder Cancer Infrastructure Foundation
Other
Prospective Bladder Cancer Infrastructure: an Infrastructure for Observational and Interventional Bladder Cancer Research (ProBCI)
Acronym: ProBCI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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