White Light Scanning to Aid Body Contouring: A Pilot Project

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Lipodystrophy
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Brief Title

White Light Scanning to Aid Body Contouring: A Pilot Project

Official Title

White Light Scanning to Aid Body Contouring: A Pilot Project

Brief Summary

      A white light scanner can more accurately measure body contouring subjects than standard
      anthropomorphic methods.

Detailed Description

      A 3-D digital body camera that employs non-intrusive white light phase profilometry and 24
      coordinated charge-coupled cameras scans and produces a "point cloud" image of the subject.
      The result of the two-minute scan process is an accurate three-dimensional body model of the
      subject, consisting of over 1.2 million surface points. The point cloud is compressed to
      provide programmable measurement extraction profiles (MEP's) that automatically extracts
      linear and circumferential measurements. Subjects are scanned and anthropometrically measured
      pre-operatively, and at 3, 6 and 9 months post-op.

Study Type

Observational

Primary Outcome

To study whether the scanner was faster and more accurate than anthropometric measurements.

Condition

Lipodystrophy

Study Arms / Comparison Groups

 PROSPECTIVE BODY CONTOURING SUBJECTS
Description:  It is anticipated that the participants will undergo body contouring procedures including lipoplasty [internal fat suction removal], abdominoplasty [surgical removal of lower abdominal skin and fat], breast reduction [surgical removal of breast skin, fat, and breast tissue to reduce breast size], breast augmentation [surgical breast enlargement], thigh lift [surgical removal of upper thigh tissue], and brachioplasty [surgical removal of upper arm tissue].
These procedures will be evaluated by pre- and post-operative digital scans, analog measurements, and clinical examinations and photographs.

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Estimated Enrollment

500

Start Date

January 2005

Completion Date

October 2020

Primary Completion Date

August 2020

Eligibility Criteria

        Inclusion Criteria:

          -  All healthy preoperative body contouring subjects between 18-65 years old are
             potentially included in this study.

        Exclusion Criteria:

          -  Pregnant, nursing,or have a history of epilepsy.

          -  Individuals under 18 years old;

          -  Problems reading or understanding spoken instructions;

          -  Are in jail or in a "locked ward";

          -  Are a student or an employee of EVMS; or

          -  Are chemically-dependent.

Gender

All

Ages

18 Years - 80 Years

Accepts Healthy Volunteers

Accepts Healthy Volunteers

Contacts

David A Gilbert, MD, 757-274-4000, [email protected]

Location Countries

United States

Location Countries

United States

Administrative Informations

NCT ID

NCT01093950

Organization ID

05-09-FB-0235

Responsible Party

Principal Investigator

Study Sponsor

Eastern Virginia Medical School

Collaborators

 Novaptus Systems Incorporated

Study Sponsor

David A Gilbert, MD, Principal Investigator, Eastern Virginia Medical School

Verification Date

October 2014