Clinical Trials

Overview

About this study

The correction of breast asymmetries requires the capture of accurate surface images and anatomical measurements of the breast.  Currently, surface breast measurements are performed manually.  We hypothesize that using the true depth imaging sensors embedded within mobile devices and differential algorithms, breast measurements can be performed in an automated format.  These measurments can be potentially utilized for the production of asymmetric garments to improve comfort and symmetry.

The study plans to include female subjects (ages 18 – 85) previously evaluated for aesthetic and reconstructive breast surgery and add new subjects who desire aesthetic or reconstructive breast surgery in the future.  This study involves the collection of data through noninvasive measurements.

The methodology involves comparing the accuracy of breast measurements using a custom developed mobile application with routine measurements obtained manually on physical examination and from the Canfield Vectra 3D imaging platform.  Standardized anatomical measurements will be taken of the patient’s breast using three methods: (1) manually, (2) the Canfield Vectra 3D platform and (3) the mobile application.   In addition, volume breast measurements will be obtained using the Canfield platform and the mobile application.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Participating Mayo Clinic locations

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