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White Light Scanning to Aid Body Contouring: A Pilot Project

White Light Scanning to Aid Body Contouring: A Pilot Project

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01093950
Enrollment
500
Registered
2010-03-26
Start date
2005-01-31
Completion date
2020-10-31
Last updated
2014-10-09

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

Conditions

Body Dysmorphic Disorders, Lipodystrophy

Keywords

anthropometric, white light scanner, extraction profiles, Body lipodystrophy

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.

Interventions

None listed

Sponsors

Novaptus Systems Incorporated
CollaboratorINDUSTRY
Eastern Virginia Medical School
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
To study whether the scanner was faster and more accurate than anthropometric measurements.9 monthsThe scanner and anthropometric measurements will be compared for accuracy and fidelity of collection. Anthropometric tape measurements will be compared to measurement extraction profiles provided by the scanner.Conclusions will be drawn based on the data collected.

Countries

United States

Contacts

Primary ContactDAVID A GILBERT, MD
Dagilb3@msn.com757-274-4000
Backup ContactROBERT H SCHNARRS, MD
HAGUE400@AOL.COM757-274-4000

Outcome results

None listed

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