Thermalogical Analysis of a Cohort of Women and Men Undergoing Mammographic Analysis.

This study is designed to evaluate the Sentinel BreastScan II as well as the analysis of data by Therma-Scan.

Study Overview

• Status: Suspended
• Conditions: Breast Neoplasm Female; Cancer, Breast; Thermography
• Intervention / Treatment: Device: Sentinel BreastScan II

Detailed Description

FirstSense Medical, LLC is a medical device company which has developed a breast cancer screening device, the Sentinel BreastScan II [SBS II]. This radiation free device is being developed to produce data which will be analyzed by Therma-Scan Reference Laboratory. Dr. Hoekstra, CEO of Therma-Scan, is the author of a published paper based on breast thermal data with a reported 95% sensitivity and 91% specificity. The SBS II examination will take approximately 7 minutes.

This study is designed to evaluate the Sentinel BreastScan II as well as the analysis of data by Therma-Scan. SBS II thermal breast data is an adjunctive aid to standard breast imaging. Currently, mammography is one of the standards of care in screening for visible signs of breast cancer. Breast thermology is the analysis of the heat signature data from an examined breast. All study costs will be incurred by the sponsor. Study subjects will incur no cost to participate. All scientific data revealed in this protocol will be used for the specific objectives of the study. The SBS II is a non-significant risk device. There is no contact with the subject during the entire procedure.

• Study Type: Observational
• Enrollment (Anticipated): 2000

Contacts and Locations

Study Locations

• United States
  • Ohio
    • Toledo, Ohio, United States, 43614
      • Eleanor N. Dana Cancer Center, University of Toledo

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

Study population consists of any patient undergoing standard mammographic examination and/or any additional imaging study predicated on the results of mammography.

Description

Inclusion Criteria:

• Male or Female, over the age of 18 years of age.
• Asymptomatic women or women who are being screened for breast abnormality.
• Women scheduled for a mammogram or women who have had a mammogram and are given 3 days to wait in between their mammogram and scheduled biopsy and FS/TS system.
• Not pregnant or breast feeding.
• Signed Informed consent.

Exclusion Criteria:

• Subject does not meet inclusion criteria, noted above.
• Use of 100 mg or more of niacin by tablet or niacin patch within the last 24 hours.
• Use of nitroglycerin within the last 24 hours.
• Subject experienced a fever of 102°F or higher within thirty-six (36) hours of the study.
• Subject must not have had a mammogram, breast ultrasound, or breast exam within the last 72 hours prior to the SBS II.

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort

Intervention / Treatment

SBS II

Device: Sentinel BreastScan II; The SBS II will automate the recording of thermal data used in the Therma-Scan manual thermology protocol by utilizing a thermal camera sensitive to changes in breast temperature. The SBS II system uses a very sensitive thermography camera that detects and visually displays heat patterns that naturally emanate from the breast. SBS II captures this data digitally for subsequent analysis by Therma-Scan.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Measure protocol accuracy	To measure the sensitivity and specificity of thermographic analysis based on the Marseilles analytic protocol [ Th 1 thru 5 ] to biopsy results predicated on standard breast imaging criteria [ BIRADS analytical protocol, B1 thru B5 ]. The resultant BIRADS score and biopsy pathological results will be compared to thermographic analysis [ Th1 thru 5 ] for each subject. 50 subjects undergoing both thermography and standard breast imaging leading to biopsy [ BIRADS 3 thru 5 ] will then be compared by measuring the results of each, BIRADS for standard breast imaging v the Marseilles Th system used in thermographic analysis, for concordance or discordance of findings as measured on final pathological analysis. This analysis will be performed for each subsequent 50 patient cohort undergoing standard mammographic/ultrasound breast imaging analysis.	Through study completion, an average of 4 years.

Collaborators and Investigators

• Sponsor: First Sense Medical, LLC
• Collaborators: University of Toledo Health Science Campus
• Investigators: Principal Investigator: Haitham Elsamaloty, University of Toledo

Study record dates

Study Major Dates

• Study Start (Actual): November 3, 2017
• Primary Completion (Anticipated): September 1, 2021
• Study Completion (Anticipated): September 1, 2026

Study Registration Dates

• First Submitted: July 24, 2017
• First Submitted That Met QC Criteria: August 31, 2017
• First Posted (Actual): September 5, 2017

Study Record Updates

• Last Update Posted (Actual): January 10, 2018
• Last Update Submitted That Met QC Criteria: January 8, 2018
• Last Verified: January 1, 2018

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Skin Diseases; Neoplasms; Neoplasms by Site; Breast Diseases; Breast Neoplasms
• Other Study ID Numbers: SBS-001

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: Yes
• product manufactured in and exported from the U.S.: No