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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05195515
Other study ID # CONQUER
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date December 31, 2027

Study information

Verified date July 2023
Source Aarhus University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 2000
Est. completion date December 31, 2027
Est. primary completion date December 31, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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 Design


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Department of Urology, Aarhus University Hospital Aarhus N
Denmark Department of Urology, Regional Hospital Gødstrup Gødstrup
Denmark Department of Urology, Regional Hospital Horsens Horsens
Denmark Department of Urology, Regional Hospital Randers Randers
Denmark Department of Urology, Regional Hospital Viborg Viborg

Sponsors (3)

Lead Sponsor Collaborator
Aarhus University Hospital Aarhus University, Institute of Clinical Medicine, National Research Center for Survivorship and Late Adverse Effects Following Pelvic Organ Cancer, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Health-related Quality of Life Changes in Quality of Life measured using validated instruments 5 years from baseline inclusion
Secondary Prevalence of late effects Based on Patient Reported Outcomes and medical records 5 years from baseline inclusion
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