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NCT07581496Recruiting

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

Source: ClinicalTrials.gov · Last updated 18 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
35 (estimated)
First submitted
5 May 2026
Start date
18 Jun 2025
Primary completion date
1 Jun 2030
Lead sponsor
University Hospital, Basel, Switzerland
NCT number
NCT07581496

What you commit to

  • Study type: Observational
  • Planned participants: 35
  • From 18 Jun 2025 to the primary completion date, 1 Jun 2030
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with metastases or concomitant upper tract tumor at diagnosis will

Other illness

  • Patients with non T1 G3 cancers
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.

Age

  • Vulnerable persons (e.g. \< 18y of age, unable to consent to the study)

Other

  • Patients with upstaging, either at re-TUR-B or after immediate radical cystectomy

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitätsspital Basel
Coordinator of this site? Confirm its status
BaselSwitzerlandRecruiting
Luzerner Kantonsspital
Coordinator of this site? Confirm its status
LucerneSwitzerlandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.