Skip to main content
Clinical Trials/NCT04655300
NCT04655300
Completed
Not Applicable

Evaluation of Age-related Skin Changes Using Clinical Probe Measurements and Imaging Modalities in Chinese Subjects

Allergan1 site in 1 country102 target enrollmentJanuary 16, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Age-related Skin Changes
Sponsor
Allergan
Enrollment
102
Locations
1
Primary Endpoint
Age-related changes in skin hydration on the cheeks, forehead, neck and around the mouth
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Evaluation of age-related skin changes using clinical probe measurements and imaging modalities in Chinese subjects.

Registry
clinicaltrials.gov
Start Date
January 16, 2021
End Date
February 5, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Allergan
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Chinese subjects
  • Subject agreeing to complete all study required procedures.
  • Subject having given freely and expressly his/her informed consent.

Exclusion Criteria

  • Pregnant or nursing woman or planning a pregnancy during the study.
  • Subject who had been deprived of their freedom by administrative or legal decision or who is under guardianship.
  • Subject in a social or sanitary establishment.
  • Subject participating to another research on human beings or being in an exclusion period for a previous study.
  • Intensive exposure to sunlight or UV-rays within the previous month and foreseen during the study.
  • Subject who underwent tissue augmentation with dermal fillers including HA, calcium hydroxylapatite, autologous fat, mesotherapy, or other cosmetic procedures (eg, face-lift, laser, photomodulation, intense pulsed light, radiofrequency, dermabrasion, chemical peel, or other ablative procedures) in the face within 12 months before study entry or was planning to undergo any such treatment during the study.
  • Subject who underwent treatment with botulinum toxins in the face or neck within 6 months of study entry or was planning to undergo such treatment during the study.
  • Subject who ever received semi-permanent fillers or permanent facial implants (eg, poly-L-lactic acid, polymethylmethacrylate, silicone, expanded polytetrafluoroethylene) anywhere in the face or was planning to be implanted with any of these products at any time during the study.
  • Subject with current cutaneous inflammatory or infectious processes (eg, acne, herpes), abscess, an unhealed wound, or a cancerous or precancerous lesion on the face that could interfere with measurements.
  • Subject having changed, started or stopped any hormonal treatment or any treatment likely to have an impact on skin condition (over-the-counter or prescription, oral or topical, anti-wrinkle products on the face), within 30 days prior to enrollment or is planning to begin using such products during the study.

Outcomes

Primary Outcomes

Age-related changes in skin hydration on the cheeks, forehead, neck and around the mouth

Time Frame: 2 Months

Skin hydration will be measured using tissue dielectric constant measurement. Tissue dielectric constant is expressed as a unitless value that is directly proportional to the amount of water in the tissue.

Age-related changes in skin elasticity on the cheeks, forehead and neck

Time Frame: 2 Months

Skin elasticity measurement using suction based device

Age-related changes in skin color on the cheeks and forehead

Time Frame: 2 Months

Skin colorimetric measurement will be done with a Spectrophotometer

Age-related changes in skin thickness on the cheek

Time Frame: 2 Months

Epidermal thickness will be measured with an optical coherence tomography instrument

Age-related changes in skin blood flow on the cheek

Time Frame: 2 Months

Blood Flow (redness) will be measured with an optical coherence tomography instrument

Age-related changes in skin roughness on the cheek

Time Frame: 2 Months

Skin surface roughness will be measured with an optical coherence tomography instrument

Age-related changes in skin OAC on the cheek

Time Frame: 2 Months

Optical Attenuation Coefficient (OAC) will be measured with an optical coherence tomography instrument

Age-related changes in skin topography on the cheeks, forehead and around the mouth

Time Frame: 2 Months

Skin topography imaged using a using a fringe projection imaging system. Output measurements from the images will include Ra (average roughness), Rq (Root Mean Square of the profile heights), RMax (Maximum Roughness Depth), Rv (Depth of the Largest Profile Valley), Rvm (Average depth of the Profile Valleys), Rz (average height of roughness) and Rt (maximum height of the roughness profile)

Age-related changes in gloss/shine, pores, skin color and texture on the cheek, forehead and around the mouth

Time Frame: 2 Months

Skin gloss (Shine, pores, skin color and texture ) imaged using a camera-based system which uses various lighting/capture modalities to enhance the visualization of skin features

Clinical scoring of age-related changes in fine lines on the cheek

Time Frame: 2 Months

The investigator will assess the participant's appearance of fine lines/wrinkles using a 5-point scale from (0=None to 4=Diffuse)

Clinical scoring of age-related changes in skin roughness on the cheek

Time Frame: 2 Months

The investigator will assess the participant's appearance of skin roughness using a 5-point scale from (0=None to 4=Diffuse)

Secondary Outcomes

  • To correlate the age-related skin hydration measurements on the cheeks, forehead, neck and around the mouth to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related skin elasticity measurements on the cheeks, forehead and neck to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related skin color measurements on the cheeks and forehead to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related skin thickness measurements on the cheek to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related skin blood flow measurements on the cheek to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related skin roughness measurements on the cheek to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related skin OAC measurements on the cheek to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related skin topography measurements on the cheeks, forehead and around the mouth to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related gloss/shine, pores, skin color and texture on the cheek, forehead and around the mouth to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related fine lines on the cheek to clinical scoring of fine lines and skin smoothness.(2 Months)
  • To correlate the age-related skin roughness on the cheek to clinical scoring of fine lines and skin smoothness.(2 Months)
  • Age-related changes and repeatability in the perioral area for hydration and topography.(2 Months)
  • Age-related changes and repeatability in the neck for hydration and elasticity.(2 Months)
  • Age related changes and repeatability in the forehead for hydration, color, elasticity, topography, skin gloss, color, texture, pores.(2 Months)

Study Sites (1)

Loading locations...

Similar Trials