Actively Recruiting

Age: 20Years - 35Years
All Genders
Healthy Volunteers
ID06732609

Clinical Evaluation and Characterization of Normal Perioral Tissue Using Advanced Videodermoscopy A Pilot Study on Dental Students

Led by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Updated on 2024-12-13

80

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting an observational pilot study to carefully examine the normal skin and mucosal structures around the mouth in healthy young adults aged 20 to 35 years. The study aims to document details like pores, fine lines, texture, pigmentation, vascular patterns, and skin irregularities in specific areas such as the anterior chin, vermilion border, and vermilion zone. This detailed evaluation introduces new imaging findings to better understand the complex features of healthy perioral tissue. The study uses advanced imaging tools, including the Horus 1000VMF system with two dermatoscopic probes at 30x and 150x magnification and a Fluorescence Advanced Videodermatoscopy (FAV) probe at 500x magnification. These devices capture detailed images under different light modes to observe surface and deeper skin layers. Before imaging, the skin is cleaned and treated with glycerol for clarity. Images from three key mouth areas are taken, stored, and independently reviewed by trained investigators. Participants will have their perioral region imaged and assessed over 8 weeks, with the research team analyzing characteristics like mucosal health, surface texture, and skin features using specialized classifications for skin type and phototype. Data on age, sex, and skin type are also collected to provide a comprehensive picture. The study carefully monitors participants to ensure consistent, unbiased image analysis, supporting future research on perioral skin.

CONDITIONS

Brief Title

Perioral Tissue Evaluation With Advanced Videodermoscopy (FAV)

Who Can Participate

Age: 20Years - 35Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants must be between 20 and 35 years old
  • Must be in good general health with no known systemic diseases (ASA I)
  • Must have clinically healthy skin in the target area with no history of eczema, psoriasis, or dermatitis
  • Must provide written informed consent to participate
  • Must be non-smokers or have quit smoking for at least 12 months
  • Must not have had recent skin treatments (laser, chemical peels, topical meds) in the area within the last 3 months
Not Eligible

You will not qualify if you...

  • History of skin diseases like acne, psoriasis, eczema, or other interfering skin conditions
  • Presence of chronic systemic illnesses such as diabetes or autoimmune diseases
  • Current use of medications that could alter skin (corticosteroids, retinoids, immunosuppressants)
  • Known allergies to topical products used during examination
  • Pregnant or breastfeeding individuals
  • Recent dermatological procedures in the area within the last 3 months
  • Recent excessive sun exposure or sunburns in the target area within the last 2 months
  • Unwillingness or inability to follow study procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 8 weeks

Participants undergo detailed imaging and clinical evaluation of the perioral tissue using advanced videodermoscopy and fluorescence techniques.

1 to 3 visits for image acquisition and evaluation

Long-term Monitoring

Duration - Up to 8 weeks

Participants' perioral tissue images and characteristics are monitored and analyzed over time to assess variability and stability of skin features.

Follow-up assessments as scheduled within 8 weeks

Trial Site Locations

Total: 1 location

1

UOC Clinica Odontoiatrica, Fondazione Policlinico Agostino Gemelli IRCCS

Roma, Italy, 00168

Actively Recruiting

Loading map...

Research Team

A

Andrea Camodeca, DMD, MSc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Similar Trials

Prevalence of Oral Mucosal Lesions Among a Sample of Adult E...

Oral Mucosal Disease

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial