Menu
Enrolling by invitation NCT05195515

The Impact of Late Effects After Treatment for Bladder Cancer on Quality of Life

Observational Bladder Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Bladder Cancer. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Denmark
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Impact of Late Effects After Treatment for Bladder Cancer on Quality of Life - What is the Cost of the Cure?

Overview

Bladder Cancer prognosis, treatment, and subsequent morbidity and mortality vary between the different stages, thus resulting in a different impact on patients' lives. There are some well known late effects of the treatments for bladder cancer, but the knowledge of their impact on patients Quality of Life is sparse. This study aims to determine the prevalence of late effects impact on Quality of Life and potential risk factors for impairment.

Primary outcome measures

  • Health-related Quality of Life [Time frame: 5 years from baseline inclusion]
Secondary outcome measures (1)
  • Prevalence of late effects [Time frame: 5 years from baseline inclusion]

Eligibility criteria

Inclusion criteria

  • Patients are eligible if they are referred to a hospital in the Central Region Denmark, due to hematuria between 01/01/2022 and 01/01/2023
  • Ability to understand written and oral Danish

Exclusion criteria

  • Known Alzheimers disease
  • Diagnosed other causes explaining the hematuria

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Denmark · 5 centers
  • Department of Urology, Aarhus University Hospital — Aarhus N
  • Department of Urology, Regional Hospital Gødstrup — Gødstrup
  • Department of Urology, Regional Hospital Horsens — Horsens
  • Department of Urology, Regional Hospital Randers — Randers
  • Department of Urology, Regional Hospital Viborg — Viborg

Identifiers

NCT: NCT05195515 · CONQUER

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗