Evaluation the Feasibility of the FOSTI Device
This trial is active, not recruiting.
|Start date||March 2008|
|Trial size||50 participants|
|Trial identifier||NCT00791609, OpVe-HI-08-001|
Feasibility of accurate differentiation between malignant and benign tissue using the FOSTI device on surgically removed tissue
Male or female participants of any age.
Inclusion Criteria: - Subjects of all ages. - Subject is able, agree and sign the Informed Consent Form. Exclusion Criteria: - Subject has any conditions, which precludes compliance with study
|Official title||Evaluation the Feasibility of the FOSTI Device Accurately and in a Real Time Way to Differentiate Malignant From Benign Tissue (Performed ex Vivo) in Cancer Surgery|
|Description||Characterization of the optical fiber sensor's interaction with the tissue. Creating a database of tissue lesions and their 'optical signature' (lesion classifier). Optimization of the FOSTI device by minimizing the false-positive and false-negative results.|
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