Bladder Cancer Clinical Trial
Official title:
Bladder Cancer Prognosis Programme (Incorporating SELENIB Trial)
Verified date | October 2007 |
Source | National Cancer Institute (NCI) |
Contact | n/a |
Is FDA regulated | No |
Health authority | Unspecified |
Study type | Interventional |
RATIONALE: Studying different factors that effect patients with newly diagnosed bladder
cancer may help doctors learn more about the disease, improve the ability to plan cancer
treatment, and help patients live more comfortably.
PURPOSE: This clinical trial is studying different factors affecting patients with newly
diagnosed bladder cancer.
Status | Recruiting |
Enrollment | 3400 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
DISEASE CHARACTERISTICS: - Bladder lesion with cystoscopic characteristics compatible with urothelial cancer or transitional cell carcinoma meeting 1 of the following criteria: - Non-muscle-invasive tumor - Muscle-invasive tumor - Solitary G1 pTa tumor - No previous diagnosis of cancer of the urethra, bladder, ureter, or renal pelvis within the 10 years prior to current diagnosis PATIENT CHARACTERISTICS: - Fit for cystoscopy and surgical biopsy/resection - No HIV infection - No condition that, in the opinion of the local investigator, might interfere with the safety of the patient or evaluation of the study objectives PRIOR CONCURRENT THERAPY: - Not specified |
Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United Kingdom | Queen Elizabeth Hospital at University Hospital of Birmingham NHS Trust | Birmingham | England |
Lead Sponsor | Collaborator |
---|---|
University Hospital Birmingham |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Recurrence-free interval | |||
Primary | Progression-free interval | |||
Secondary | Overall survival time | |||
Secondary | Incidence of transitional cell carcinoma outside the bladder | |||
Secondary | Incidence of all other malignancies clinically diagnosed | |||
Secondary | Incidence of cardiovascular events | |||
Secondary | Quality of life as measured by EORTC QLQ-C30, QLQ-BLS24 and QLQ-BLM30 questionnaires |
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