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Clinical Trial Summary

Previous studies show that the majority NMIBC patients experience side effects to BCG and therefore terminate the instillations before completing all planned instillations. This will increase their risk of recurrence and potential cystectomy. The purpose of this study is to investigate if NMIBC patients who experience severe side effects to BCG instillations will experience fewer or less severe side effects if reducing dwell-time of BCG instillations. The study will include patients from Denmark, Iceland, Norway and Sweden.


Clinical Trial Description

Approximately 8,000 patients are diagnosed with bladder cancer (BC) in the Nordic countries every year. The majority of BC patients are diagnosed with non-muscle invasive bladder cancer (NMIBC). The majority of NMIBC are treated with Bacillus Calmette-Guérin vaccine (BCG) as adjuvant treatment but for carcinoma in situ it is the primary treatment. BCG is known to give a lot of side effects both local and systemic, the severity of these can lead to premature termination of the treatment. The object of this PhD project is to investigate if reduced dwell time, the time the BCG is in the bladder, will decrease the severity of side effects due to BCG instillations. This will be investigated in a Nordic setting and the project will be done as a two-armed randomized clinical trial. By decreasing the severity of side effects, we hypothesize the number of patients completing all planned instillations will increase and thereby decrease the risk of the BC evolving into a more aggressive type. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04701151
Study type Interventional
Source Aarhus University Hospital
Contact Jørgen B. Jensen, Professor,DMSc
Phone +45 78452617
Email Bjerggaard@skejby.rm.dk
Status Recruiting
Phase Phase 4
Start date February 3, 2021
Completion date December 2030

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