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Study To Investigate If Embody's Retinol Gummies Improve The Early Signs Of Skin Aging And Overall Skin Health

Study to Identify if Embody's Retinol Gummy Works to Improve the Appearance of Early Signs of Aging and to Examine if it Reduces the Overall Frequency and Intensity of Adult Acne.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04884516
Enrollment
35
Registered
2021-05-13
Start date
2021-01-19
Completion date
2021-04-15
Last updated
2021-05-13

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

Conditions

Acne, Adult

Keywords

skin aging, adult acne

Brief summary

The Embody retinol study is a single-arm clinical trial on skin aging prevention and adult acne. The purpose of this study is to determine the effect of a retinol gummy in adults aged 18-45 on skin aging and overall skin health.

Detailed description

Embody has developed a retinol gummy with the aim to improve the appearance of early signs of aging, such as fine lines, dark spots, and sagging. Embody's retinol gummy has also the goal to reduce the overall frequency of adult acne and an improvement of overall skin health by promoting hydrated, brightened skin. The study aims to collect self-reported outcomes and photographic images to understand the assessment of the efficacy of treatment from the participant's perspective, and if participants see an improvement in their fine lines, wrinkles, dark spots, and sagging.

Interventions

DIETARY_SUPPLEMENTRetinol gummy

Participants take one retinol gummy per day

Sponsors

Citruslabs
CollaboratorINDUSTRY
Embody Beauty, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Male or female between 18-45 years old * Must be in good general health * May experiences adult acne and/or early-stage wrinkles that are not treated by topical or oral prescription drugs/medication * Must maintain a basic skincare routine * Must discontinue the use of other dietary supplements * Must be willing to comply with the requirements of the protocol * Is able to communicate in English * Is willing to skip their normal skincare routine * Must provide written informed consent form (ICF) * Is willing and able to share feedback and take skin pictures via the used technology portal

Exclusion criteria

* Unwilling to provide consent * Unwilling to skip their normal skincare routine * Unwilling to follow the routine of the protocol * Use of other oral retinoids * Use of prescription medication relevant to the skin * Undergoing any cosmetic procedures during the study including Botox, laser or chemical treatments * Deep-set of wrinkles * History of the following medical conditions or diseases: * Kidney disease * Liver disease * Alcohol abuse * Use of prescription drug (topical or oral) that is targeted at any sort of skin condition (for example retinoids) * Any known allergies/sensitivities to nuts

Design outcomes

Primary

MeasureTime frameDescription
Skin aging [Time frame: Baseline to 8 weeks]8 week intervention periodPatient reported outcome measures (Scale 0-5 with higher scores representing a better outcome) to assess the reduction of early signs of aging such as fine lines, dark spots, and sagging
Adult acne [Time frame: Baseline to 8 weeks]8 week intervention periodReduction the overall frequency and intensity of adult acne (Scale 0-5 with higher scores representing a reduction in the appearance of adult acne)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026