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Prospective Study of Topical Adapinoid Versus Topical Retinol

Prospective, Double-Blinded, Randomized Head-to-Head Study of Topical Adapinoid Versus Topical Retinol

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05778760
Enrollment
48
Registered
2023-03-21
Start date
2023-05-01
Completion date
2023-09-01
Last updated
2024-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wrinkle

Keywords

anti-aging, skin care

Brief summary

This study is to analyze and compare the effects of applying two topical vitamin-A derived ingredients on facial skin health, appearance and tolerability. One of these ingredients is retinol, and the other is Adapinoid, also known as Oleyl Adapalenate, a novel anti-aging ingredient.

Detailed description

We want to assess the effect of applying vitamin A-derived ingredients on facial skin health, appearance, and tolerability. One of these ingredients is retinol, and the other is Adapinoid, also known as Oleyl Adapalenate. In this study, participants will be randomized to either receiving a retinol product, or an Adapinoid product and they will be assessed at three follow up visits at week 4, week 8, and week 12.

Interventions

OTHERRetinol

Topical retinol (0.5%) applied to the face

OTHERAdapinoid

Topical Adapinoid (0.5%) applied to the face

Sponsors

Actera (Sponsor)
CollaboratorUNKNOWN
Integrative Skin Science and Research
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
35 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Men and women between the ages of 35 years old and 65 years old

Exclusion criteria

* Individuals who are pregnant or breastfeeding. * Prisoners. * Adults unable to consent. * Individuals who have changed any of their hormonal based contraception within 3 months prior to joining the study. * Subjects using any topical retinoid, acetyl zingerone, vitamin C, bakuchiol, hyaluronic acid or benzoyl peroxide containing topical product within 2 weeks of starting study or any subject unwilling to refrain from washout prior to enrollment. * Subjects with any of the following facial cosmetic treatments in the past 3 months or those who are unwilling to withhold the following facial cosmetic treatments during study including botulinum toxin, injectable fillers, microdermabrasion, intense pulsed light (IPL), peels, laser treatments, acid treatments, facial plastic surgery, or any other medical treatment administered by a physician or skin care professional which is designed to improve the appearance of facial skin. * Current tobacco smoker or a tobacco smoking history of greater than 10 pack-years.

Design outcomes

Primary

MeasureTime frameDescription
Facial fine lines and wrinkles12 weeksChange in severity of fine lines and wrinkles measured by photographic analysis (BTBP 3D Camera System)

Secondary

MeasureTime frameDescription
Facial fine lines and wrinkles4 weeksChange in severity of fine lines and wrinkles measured by photographic analysis (BTBP 3D Camera System)
Skin redness4 weeksChange in the appearance of skin redness measured by photographic analysis (BTBP 3D Camera System)
Facial skin pigment evenness4 weeksChange in the appearance of facial skin pigment intensity measured by photographic analysis (BTBP 3D Camera System)
Self-perception of skin health and appearance4 weeksSurvey-based self-assessment of aspects of skin health and appearance
Tolerability of product4 weeksQuestionnaire based self-assessment about the tolerability of the topical skin product

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026