Evaluation the Feasibility of the FOSTI Device

Optivasive

Status: Unknown

Conditions: Cancer

Study type: Observational

Funder types: Industry

Identifiers

NCT00791609

OpVe-HI-08-001

Details and patient eligibility

About

Feasibility of accurate differentiation between malignant and benign tissue using the FOSTI device on surgically removed tissue

Full 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.

Enrollment: 50 patients

Sex: All

Volunteers: Accepts Healthy Volunteers

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