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Facial Asymmetrical Clinical Evaluation Study

NCT03347747 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2017-11-20

No results posted yet for this study

Summary

The primary objective of this study is to create digital 3D images of subjects using a Canfield VECTRA H1 digital imaging system and compile a medical, skin/sun exposure and sunscreen use, and skin care product history for a large number of subjects. This data will allow for image and statistical analysis to determine if facial volume loss is greater on one side, and what factors may be causing this.

The data collected will also serve as a database for future lines of inquiry relating to data collected in this study. Your data (including 3D images) will be kept in this database and may be accessed in the future by any Sponsor or Investigator. Your data will be de-identified and your name will not be associated with the questionnaire responses

Conditions

  • Loss of Facial Adipose Tissue

Interventions

OTHER

Study Photography + Personal & Medical History Collection

3D facial images taken and complete a detailed study questionnaire

Sponsors & Collaborators

  • Allergan

    collaborator INDUSTRY

  • Merz Aesthetics Inc.

    collaborator INDUSTRY

  • ThermiGen, LLC

    collaborator INDUSTRY

  • McDaniel Institute of Anti-Aging Research

    lead INDUSTRY

Principal Investigators

  • Daivd H. McDaniel, MD · MIAAR

Eligibility

Min Age
45 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-06-09
Primary Completion
2018-06-30
Completion
2018-07-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03347747 on ClinicalTrials.gov