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Taking people in SwitzerlandNo phase

Detecting tumor DNA in blood and urine of people with early bladder cancer

Checks for tumor DNA in urine and blood of adults with early bladder cancer.

Plain-language title generated from the registry record
Registry title: T1G3R-1 Trial: Detectability and Prognostic Value of ctDNA in T1 G3 Bladder Cancer

Key facts

Where
Basel and Lucerne, SwitzerlandSee the 2 sites

Where in Switzerland

  • Universitätsspital BaselBasel, SwitzerlandTaking people
  • Luzerner KantonsspitalLucerne, SwitzerlandTaking people

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  4. What happens if I want to stop?
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Trial details

Who runs it
University Hospital, Basel, Switzerland
Trial code
NCT07581496
Record updated
18 May 2026
Original description
T1G3 bladder cancer is a heterogeneous disease with a high risk of disease persistence after the first TUR-B, understaging, disease progression, bladder removal, and mortality.Read full original descriptionShow less

T1G3R-1 Trial: Detectability and Prognostic Value of ctDNA in T1 G3 Bladder Cancer

T1G3 bladder cancer is a heterogeneous disease with a high risk of disease persistence after the first TUR-B, understaging, disease progression, bladder removal, and mortality.

Current risk stratification is insufficient and needs improvement. Ct-DNA could identify patients with disease persistence, progression and could monitor and tailor therapy. It might improve patient risk stratification, avoiding under- and overtreatment, reducing morbidity and mortality.

Primary objective is to investigate the detectability of ct-DNA in T1G3 urothelial bladder cancer patients and build a biobank through collection of different sample types (urine, plasma) in T1G3 bladder cancer patients which allows future retrospective testing.

Inclusion: patients > 18 years of age, able to give informed consent as documented by signature,; patients with a cystoscopically proven bladder cancer, suspicious for T1 stage, who will undergo TUR-B.

Exclusion: Patients with metastases or concomitant upper tract tumor at diagnosis will; Patients with non T1 G3 cancers; Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc; Vulnerable persons (e.g. < 18y of age, unable to consent to the study); Patients with upstaging, either at re-TUR-B or after immediate radical cystectomy.

ClinicalTrials.gov NCT07581496