HOPE-07-MIBC: Disitamab Vedotin Plus Immunotherapy vs Chemoimmunotherapy in Resectable HER2-Expressing MIBC
NCT07608224
Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications
View Trial DetailsNCT Number: NCT07735793
The purpose of this study is to assess participant's overall well-being and the extent to which medical services are used by participants with non-muscle invasive bladder cancer (NMIBC) and muscle invasive bladder cancer (MIBC) who have undergone radical cystectomy (surgical procedure to remove entire urinary bladder). NMIBC is a type of bladder cancer in which cancer is confined to innermost lining of the bladder and MIBC is a type of bladder cancer in which cancer has grown deep into the thick muscle of the bladder.
Trial opening soon.
Get Notified19 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Up to 12 months post RC procedure
Number of participants in Cohort B reporting post-operative complications (including hemorrhage/bleeding, cardiac, respiratory, gastrointestinal, genitourinary, wound and hernia, thrombosis/embolic, infection and sepsis, renal failure, metabolic disturbances, dehydration, failure to thrive, malnutrition, neurologic, psychiatric conditions, and miscellaneous and surgical) within 12 months after RC (overall and by disease stage) will be reported.
Time frame: Up to 3 years post RC procedure
Number of participants in Cohort B reporting post-operative complications (including hemorrhage/bleeding, cardiac, respiratory, gastrointestinal, genitourinary, wound and hernia, thrombosis/embolic, infection and sepsis, renal failure, metabolic disturbances, dehydration, failure to thrive, malnutrition, neurologic, psychiatric conditions, and miscellaneous and surgical) within 3 years after RC (overall and by disease stage) will be reported.
Time frame: Up to 30 days post RC procedure
Number of deaths (mortality) amongst participants in Cohort B post-RC procedure will be reported.
Time frame: Up to 90 days post RC procedure
Number of deaths (mortality) amongst participants in Cohort B post-RC procedure will be reported.
Time frame: Up to 3 years post RC procedure
LOS for the hospitalization for RC in participants from Cohort B will be reported.
Time frame: Up to 30 days post RC procedure
Number of participants from Cohort B with readmission after RC will be reported.
Time frame: Up to 90 days post RC procedure
Number of participants from Cohort B with readmission after RC will be reported.
Time frame: Up to 12-month post RC procedure
Number of participants from Cohort B with readmission after RC will be reported.
Time frame: Up to 12 months post RC procedure
Number of hospital visits (outpatient, inpatient, and emergency) of participants from Cohort B within 12 months after RC will be reported.
Time frame: Up to 3 years post RC procedure
Number of hospital visits (outpatient, inpatient, and emergency) of participants from Cohort B within 3 years after RC will be reported.
Time frame: At Baseline
Percentage of participants from Cohort A by bladder cancer stage will be reported.
Time frame: Up to approximately 5 years
Participants receiving the different types of treatment (for example, transurethral resection of the bladder tumor [TURBT], Bacillus Calmette-Guerin [BCG], intravesical chemotherapy, radical treatment, systemic therapy, partial cystectomy, and others) during pre-RC treatment period will be reported.
Time frame: Up to approximately 5 years
Number of participants receiving intravesical chemotherapy will be reported.
Time frame: Up to approximately 5 years
Percentage of participants receiving BCG induction and maintenance therapy will be reported.
Time frame: Up to approximately 5 years
Number of BCG maintenance cycles will be reported.
Time frame: Up to approximately 5 years
Total duration of BCG therapy will be reported.
Time frame: Up to approximately 8 years
Time from diagnosis to RC amongst participants from Cohort B will be reported.
Time frame: Up to approximately 8 years
Time from last BCG to RC amongst participants from Cohort B will be reported.
Time frame: Up to 12 months post RC procedure
Participants with the occurrence of any post-RC complication within 12 months will be reported.
Time frame: Up to approximately 8 years
Total medical costs for the period from diagnosis to RC will be reported.
Time frame: Up to 30 days, 90 days, 12 months and 3 years post-RC procedure
Total medical costs for the period after RC will be reported.
Time frame: Up to approximately 8 years
Total costs for the hospitalization for RC will be reported.
Contact information is provided by the study sponsor or research team.
Janssen Korea, Ltd., Korea
Industry
Clinical and Economic Outcomes of Radical Cystectomy Among NMIBC and MIBC Patients: Nationwide Claims-Based Study in Korea
Acronym: BC RC DB
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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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