Clinical Trials Directory

Trials / Unknown

UnknownNCT01043055

Evaluation the Diagnostic Ability of the Cancer Detection Technology (CDT) to Detect Breast Cancer Among Women Population Over Age 40

Evaluation the Diagnostic Ability of the CDT to Detect Breast Cancer Among Women Population Over Age 40

Status
Unknown
Phase
Study type
Observational
Enrollment
140 (estimated)
Sponsor
Hadassah Medical Organization · Academic / Other
Sex
Female
Age
40 Years – 90 Years
Healthy volunteers
Accepted

Summary

This study aimed to validate the diagnostic ability of the CDT (cancer detection technology) software to detect breast cancer among women population.

Detailed description

Breast cancer diagnosis is a rapidly expanding research field, whose early-stage detection may reduce the burden of the disease and permit more effective treatment. It is well documented that tumor growth requires specific conditions for its development from the occurrence of a mutation to a clinically detectable cancer. It has been shown that living peripheral blood mononuclear cells (PBMC) have different ability of cytosolic enzymes (esterases) to convert hydrophobic substrate fluorescein diacetate (FDA) into hydrophilic fluorescent fluorescein. It depends on PBMC cycle stage, size, surface state, physiological states, such as activation and apoptosis. The important step of breast cancer genesis is the early change of functional activity of cytosolic enzymes (esterases) in peripheral blood mononuclear cells. Such transformations in PBMC may be detected accurately by an existing device Flowcytometer (FACS™ MultiSET™ System, company "Becton Dickinson" GmbH, USA), where measurements of fluorescence polarization and enzymatic hydrolysis of FDA substrate are recorded. A conclusion about presentation of breast cancer among examined women is achieved by "CDT" (cancer detection technology) software, which analyzes mathematically the results of fluorescence polarization and enzymatic hydrolysis. Moreover, the combined biochemical model together with additional prognostic parameters (such as age, ethnic group, gynecological and obstetric anamnesis) increases the validity (accuracy, sensitivity and specificity) of the diagnostic conclusion. Diagnostic Solution of the CDT: 1. Mathematical processing of specific blood analysis in device Flowcytometer. 2. Mathematical evaluation of specific prognostic parameters

Conditions

Timeline

Start date
2010-01-01
Primary completion
2010-01-01
Completion
2011-01-01
First posted
2010-01-06
Last updated
2010-01-06

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01043055. Inclusion in this directory is not an endorsement.