- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05195515
The Impact of Late Effects After Treatment for Bladder Cancer on Quality of Life (CONQUER)
March 2, 2026 updated by: Jørgen Bjerggaard Jensen, Aarhus University Hospital
The Impact of Late Effects After Treatment for Bladder Cancer on Quality of Life - What is the Cost of the Cure?
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.
Study Overview
Status
Enrolling by invitation
Conditions
Study Type
Observational
Enrollment (Estimated)
2000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Aarhus N, Denmark, 8200
- Department of Urology, Aarhus University Hospital
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Gødstrup, Denmark, 7400
- Department of Urology, Regional Hospital Gødstrup
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Horsens, Denmark, 8700
- Department of Urology, Regional Hospital Horsens
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Randers, Denmark, 8900
- Department of Urology, Regional Hospital Randers
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Viborg, Denmark, 8800
- Department of Urology, Regional Hospital Viborg
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients over 18 years of age, referred due to hematuria
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Health-related Quality of Life
Time Frame: 5 years from baseline inclusion
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Changes in Quality of Life measured using validated instruments
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5 years from baseline inclusion
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of late effects
Time Frame: 5 years from baseline inclusion
|
Based on Patient Reported Outcomes and medical records
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5 years from baseline inclusion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Jørgen Bjerggaard Jensen, Professor, Department of Urology, Aarhus University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2022
Primary Completion (Estimated)
December 31, 2027
Study Completion (Estimated)
December 31, 2027
Study Registration Dates
First Submitted
January 7, 2022
First Submitted That Met QC Criteria
January 7, 2022
First Posted (Actual)
January 19, 2022
Study Record Updates
Last Update Posted (Actual)
March 3, 2026
Last Update Submitted That Met QC Criteria
March 2, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CONQUER
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.