NCT07052643

Brief Summary

The main objective of this research is to identify the focal length that allows the most accurate and reproducible 2D assessment of facial aesthetics, without introducing significant distortion. Ultimately, this will enable the establishment of a standardized photography protocol for maxillofacial and aesthetic surgery, facilitating harmonized pre- and post-operative assessments and improving communication between healthcare providers and patients.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 16, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

June 16, 2025

Completed
18 days until next milestone

First Posted

Study publicly available on registry

July 4, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2025

Completed
Last Updated

July 4, 2025

Status Verified

July 1, 2025

Enrollment Period

3 months

First QC Date

June 16, 2025

Last Update Submit

July 1, 2025

Conditions

Keywords

Facial AestheticMedical PhotographyFacial AnalysisCraniofacial MorphologyImage Standardization

Outcome Measures

Primary Outcomes (1)

  • Identify the focal length setting for optimal assessment of facial aesthetics on 2D photographs

    Attractiveness score from 1 to 5 (from very unattractive to very attractive, respectively). The images will be evaluated by 4 independent raters (2 experts: facial surgeons, and 2 non-experts) based on the focal length used: 50 mm, 85 mm, 105 mm, 135 mm, and 200 mm.

    Up to 3 months

Interventions

Evaluation of the photographs by four independent raters

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Participants in the study will be individuals aged 18 years or older, with no recent facial injuries or lesions, and who have provided written informed consent to participate.

You may qualify if:

  • Age ≥ 18,
  • Signed informed consent

You may not qualify if:

  • Facial anomalies or Wounds

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hôpital NOVO - Site Pontoise

Pontoise, France

Location

MeSH Terms

Conditions

Facial Asymmetry

Interventions

Data Collection

Condition Hierarchy (Ancestors)

Pathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Epidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Nicolas JABALLAH-MAGDELEINE

    Hôpital NOVO

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 16, 2025

First Posted

July 4, 2025

Study Start

June 16, 2025

Primary Completion

September 1, 2025

Study Completion

September 1, 2025

Last Updated

July 4, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations