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Spots Global Cancer Trial Database for Blood Test for Breast Cancer Associated Auto Antibodies - Improvement of Octava Blood Test

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Trial Identification

Brief Title: Blood Test for Breast Cancer Associated Auto Antibodies - Improvement of Octava Blood Test

Official Title: Blood Test for Breast Cancer Associated Auto Antibodies - Improvement of Octava Blood Test

Study ID: NCT02066025

Conditions

Breast Cancer

Interventions

Study Description

Brief Summary: Octava has two versions, each with a different intend of use. OctavaPink is a qualitative in vitro diagnostic test service, performed by authorized clinical laboratories. The product is used for two following indications: * Intend of Use #1: OctavaPink is indicated for women above 18 years old, who performed mammography and were determined negative for breast cancer. Being moderately sensitive (\>55% sensitivity) the test is able to detect 55% of mammography false negatives. In addition, being highly specific (\>95% specificity) it supplies additional evidence for true mammography negative result which will reduce examinees anxiety of being misdiagnosed as a result of high false negative mammography rate (10-30%) * Intend of Use #2: OctavaPink is indicated for women above 18 years old, who performed biopsy after positive mammography and the biopsy result was negative. Being moderately sensitive (\>55% sensitivity) the test is able to detect 55% of biopsy false negatives. In addition being highly specific (\>95% specificity) it supplies an additional evidence for true biopsy negative result which reduces examinees anxiety of being misdiagnosed. OctavBlue is a qualitative in vitro diagnostic test service, performed by EventusDx authorized laboratories. Intend of use of OctavBlue is the following: • OctavBlue is indicated for women above 18 years old, who performed mammography and received doubtful results. Being highly sensitive (\>95% sensitivity) the test can help to reveal 95% of positive cases; and being moderately specific (\>55% specificity) - about half of negative cases. The test is not intended to be used as a standalone diagnostic technique but to supply additional information to a physician and help deciding about the further course of diagnosis.

Detailed Description: The primary objectives - To improve the specifications of the OctavaPink test and the OctavaBlue test. The current specifications being 1. For the OctavaPink - 95% specificity and 50% sensitivity. 2. For the OctavaBlue - 50% specificity and 95% sensitivity. The study will be considered as successful in any of the below options - 1. If the new antigens incorporated in the OctavaPink chip will maintain specificity of at least 95% and increase the sensitivity to at least 85%. 2. If the new antigens incorporated in the OctavaBlue chip will maintain sensitivity of at least 95% and increase the specificity to at least 85%.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: Yes

Locations

"Carmel" Medical Center, Haifa, , Israel

Contact Details

Name: Galit Yahalom, Ph.D

Affiliation: Eventus Dx

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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