Confocal Microscopy Dual Band in the Management of Bladder Cancer
NCT ID: NCT02857634
Last Updated: 2018-10-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
3 participants
OBSERVATIONAL
2016-07-31
2016-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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Bladder tumor resection
Cellvizio dual band
Using fluorescence cytoscopy, lesions in the bladder will be resected. The samples will be immediately observed in order to keep the fluorescein effect under confocal microscopy (Cellvizio dual band). After confocal microscopy samples will be fixed in formalin and prepare for the pathologist that will confirm the diagnosis. The Cellvizio system can be used to observe a resected sample ex vivo, offering a cellular-level view of internal tissue. This technique allows the visualization of the microstructure of the tissue in real-time which may improve targeted sampling, provide earlier disease detection and help patient management. The Cellvizio system includes miniaturized optics, optical fiber bundles, high-speed scanning and advanced image processing components.
Interventions
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Cellvizio dual band
Using fluorescence cytoscopy, lesions in the bladder will be resected. The samples will be immediately observed in order to keep the fluorescein effect under confocal microscopy (Cellvizio dual band). After confocal microscopy samples will be fixed in formalin and prepare for the pathologist that will confirm the diagnosis. The Cellvizio system can be used to observe a resected sample ex vivo, offering a cellular-level view of internal tissue. This technique allows the visualization of the microstructure of the tissue in real-time which may improve targeted sampling, provide earlier disease detection and help patient management. The Cellvizio system includes miniaturized optics, optical fiber bundles, high-speed scanning and advanced image processing components.
Eligibility Criteria
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Inclusion Criteria
* Patients with a bladder carcinoma and with indication of tumor resection under Hexvix procedure.
* Patients giving consent to participate in the study
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Lille Catholic University
OTHER
Responsible Party
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Principal Investigators
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Jean-Louis Bonnal, MD
Role: PRINCIPAL_INVESTIGATOR
Service d'Urologie, Groupement des hôpitaux de l'Institut Catholique de Lille
Locations
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Groupement des Hôpitaux de l'Institut Catholique de Lille
Lomme, Nord, France
Countries
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Other Identifiers
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RC-P0035
Identifier Type: -
Identifier Source: org_study_id
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