Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Los Angeles, California 90095


Purpose:

RATIONALE: Diagnostic procedures such as cystoscopy may improve the ability to detect cancer and to determine the extent of disease. PURPOSE: Diagnostic trial to compare the effectiveness of cystoscopy using hexyl 5-aminolevulinate and two light sources in detecting carcinoma in situ in patients who have bladder cancer.


Study summary:

OBJECTIVES: - Compare blue light fluorescent cystoscopy with reconstituted hexyl 5-aminolevulinate (Hexvix®) vs white light cystoscopy for the detection of carcinoma in situ (CIS) in patients with bladder cancer. - Compare the positive and false detection rates of histologically confirmed non-CIS lesions and dysplasia by these modalities in these patients. - Compare the false detection rate of histologically confirmed CIS lesions by these modalities in these patients. - Compare the number of tumor lesions and dysplasia detected by these modalities in these patients. - Compare management of patients after evaluation with these modalities. - Determine the safety of reconstituted hexyl 5-aminolevulinate (Hexvix®) in these patients. OUTLINE: This is an open-label, multicenter study. Patients undergo bladder catheterization and instillation of reconstituted hexyl 5-aminolevulinate (Hexvix®). After 60 minutes the bladder is evacuated, and the patient undergoes cystoscopic examination of the bladder by white light and then blue light fluorescence. Biopsies are taken of all suspicious areas seen under white and/or blue light modalities, and one normal-appearing area seen under both light modalities, and papillary lesions are resected. Patients are followed at 7 days after procedure. PROJECTED ACCRUAL: A total of 420 patients will be accrued for this study within 1 year.


Criteria:

DISEASE CHARACTERISTICS: - Indication for cystoscopy for suspected or confirmed bladder cancer - Meets at least one of the following criteria: - Multiple bladder lesions - Bladder lesion greater than 3 cm - Bladder tumor of at least stage T1 - Grade 2 or 3 bladder tumor - Recurrent bladder cancer - No positive cytology obtained in the last 4 weeks - No prior G3 tumor with one set of positive random biopsies - No porphyria PATIENT CHARACTERISTICS: Age - 18 and over Performance status - Not specified Life expectancy - Not specified Hematopoietic - Not specified Hepatic - Not specified Renal - No gross hematuria Other - Not pregnant or nursing - Negative pregnancy test - Fertile patients must use effective contraception during and for 1 month after study - No known allergy to reconstituted hexyl 5-aminolevulinate or a similar compound - No concurrent condition that would preclude study compliance PRIOR CONCURRENT THERAPY: Biologic therapy - More than 3 months since prior BCG Chemotherapy - More than 3 months since prior chemotherapy - Single prior dose of chemotherapy for prevention of seeding after resection allowed Endocrine therapy - Not specified Radiotherapy - Not specified Surgery - Not specified Other - More than 30 days since prior participation in another clinical trial - No concurrent participation in another clinical trial


NCT ID:

NCT00052637


Primary Contact:

Principal Investigator
Peter Schulam, MD
Jonsson Comprehensive Cancer Center


Backup Contact:

N/A


Location Contact:

Los Angeles, California 90095
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 13, 2017

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.