Evaluation the Feasibility of the FOSTI Device

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

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00791609

Enrollment

Registered

2008-11-14

Start date

2008-03-31

Completion date

Unknown

Last updated

2008-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

cancer

Brief summary

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

Detailed 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.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

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

Outcome results