Breast Aesthetics by Three Dimensional Measures

NCT03578484 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 32

Last updated 2025-07-04

No results posted yet for this study

Summary

Traditionally the measures of the optimally aesthetic breast have been assumed to be static and to represent universal values (1). Measures developed for optimal aesthetic results in breast reduction were derived from brassiere patterns and then applied universally (2). These early and important papers still strongly influence the view of the aesthetics of the breast despite the lack of individualisation and proportion.

To create satisfying results for specific patients, optimal proportions angles and relative measures are needed for each patient. The study will clarify theses measures and provide important guidelines for surgeons.The data will also help define optimal proportional aesthetics in the individual patient.

The concept of universal beauty is unrealistic. It has always been taken for granted that aesthetic values from all cultures are similar. Using 3D scanning on volunteers of youthful age offers a complex set of data that may distinguish fine differences in aesthetic ideals in different cultures.

Little is known about how life events and life-style factors affect breast aesthetics.

To follow a population with 3D scans over 5, 10 and 15 years will allow aesthetic ratings to be correlated with life events such as pregnancy, childbirth, breast-feeding and life style factors such as smoking.

The study will improve the understanding of breast aesthetics in general, in different cultures and in relation to life events and life style factors. No similar studies have previously been performed.

Conditions

Interventions

DIAGNOSTIC_TEST

Aesthetic assessment 3D breast scanning

Vectra TM - Canfield Inc breast scan. 3D digital photography scan.

Sponsors & Collaborators

  • M.D. Anderson Cancer Center

    collaborator OTHER
  • University College of Southeast Norway

    collaborator OTHER
  • Skintech A/S

    collaborator UNKNOWN
  • Canfield Inc

    collaborator UNKNOWN
  • Oslo University Hospital

    collaborator OTHER
  • Karolinska Institutet

    collaborator OTHER
  • University of Helsinki

    collaborator OTHER
  • Sykehuset Telemark

    lead OTHER_GOV

Principal Investigators

  • Lars Johan M Sandberg, MD, FACS · STHF

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-13
Primary Completion
2032-03-20
Completion
2032-03-20

Countries

  • Norway

Study Locations

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Entities

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 NCT03578484 on ClinicalTrials.gov