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3-Dimensional Form and Soft Tissue Biomechanics of the Breast

3-Dimensional Form and Soft Tissue Biomechanics of the Breast

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00502814
Enrollment
45
Registered
2007-07-18
Start date
2003-01-31
Completion date
2011-10-31
Last updated
2012-02-22

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

Conditions

Breast Cancer

Keywords

Breast Cancer, 3-D Optical Surface Scan, Soft Tissue Biomechanics, Mechanical Testing, Skin Ultrasound, Magnetic Resonance Imaging, CT Scan

Brief summary

The goal of this clinical research study is to characterize the 3-dimensional form and mechanical properties of the breast. Researchers want to do this in order to develop new high technology tools for improving the diagnosis and treatment of breast cancer in women.

Detailed description

Patients who participate in the study will have general physical and demographic information recorded. Height, weight, age, race, menstrual status, and bra size will all be recorded. Patients will have a breast physical exam. Researchers will then perform several painless tests and imaging studies to evaluate the mechanical properties of the skin and the shape and tissue composition of the breasts. Patients in this study will go through a series of evaluations as listed below. 1. 3-D Optical Surface Scan (estimated time required: 5 minutes) The camera system with a safe scanning laser will be used to take 3-D digitized images of the breasts and chest. Multiple images may be necessary to get a complete rendering of both breasts. Each image requires less than 0.6 seconds to take. This process is similar to the routine photography currently performed on most patients. 2. Mechanical testing (estimated time required: 1 hour) A small device will be applied with the surface of the skin at several locations on the breasts. A mild suction will be applied for several seconds for each measurement. This will measure how the skin tends to stretch. The instruments used are very sensitive and provide the information needed with very small, painless amounts of movement in the skin. In addition to evaluating characteristics of the breast skin, one additional measure will be taken on the skin at the front of the forearm area to help understand your general skin qualities. 3. Skin Ultrasound (estimated time required: 15 minutes) Patients will have a cutaneous ultrasound using the 20 MHz machine and the skin thickness will be recorded in each of the domains. A trained technician will complete this exam. In addition to evaluating characteristics of the breast skin, one additional measure will be taken on the skin at the front of the forearm area to help understand your general skin qualities. 4. Breast MRI and/or CT (estimated time required: 1 hour) Some patients will be scheduled for imaging of the breasts and chest using MRI and/or CT. These images will be taken free-of-charge as they are not required for standard of care. Participation will be over once the evaluations are complete. This is an investigational study. A total of 200 patients will take part in this study. All will be enrolled at M. D. Anderson. After the first 50 patients are enrolled, the results will be studied to see if the study will continue. All will be enrolled at M. D. Anderson.

Interventions

PROCEDURE3-D Optical Surface Scan

3-D digitized images of the breasts and chest will be taken over a period of five minutes.

A small device with a mild suction will be used to measure how the skin tends to stretch.

PROCEDURECutaneous Ultrasound

Cutaneous ultrasound using a 20 MHz machine and the skin thickness will be recorded.

PROCEDUREBreast MRI and/or CT

Imaging of the breasts and chest using an MRI and/or CT scan over about one hour.

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Female 2. Greater than 18 years old. 3. Presenting complaint requires breast physical examination. 4. Free of connective tissue disorders and cutaneous malignancy on the breast. 5. Free of medical conditions that contraindicate MRI or CT scanning. 6. Willing to participate in the study and able to complete informed consent.

Exclusion criteria

1\) Patients who do not meet inclusion criteria.

Design outcomes

Primary

MeasureTime frame
Individual 3-dimensional Form and Mechanical Properties of Patient's BreastPatient participation is approximately 1 Day for breast scans and mechanical measure, as well as ultrasound and Breast MRI/CT

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026