Skip to content

An Investigation of the Effects of a Royal Jelly and Bee Venom-Derived Skin Serum on Skin Health and Signs of Aging

An Investigation of the Effects of a Royal Jelly and Bee Venom-Derived Skin Serum on Skin Health and Signs of Aging

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06148753
Enrollment
40
Registered
2023-11-28
Start date
2023-11-09
Completion date
2024-04-28
Last updated
2024-11-20

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

Conditions

Skin Health

Brief summary

This is a virtual, single-group clinical trial that will last 8 weeks. Participants will use the Manuka Health Eternal Renewal Regenerating Face Serum with Royal Jelly and Bee Venom twice daily and complete questionnaires at Baseline, Week 2, Week 4, and Week 8. Participants will also undergo skin analysis via the Optic Elite facial skin analysis system at Baseline and Week 8.

Interventions

OTHERManuka Health Eternal Renewal Regenerating Face Serum with Royal Jelly and Bee Venom

Face serum containing manuka honey, royal bee jelly, and bee venom.

Sponsors

Citruslabs
CollaboratorINDUSTRY
Manuka Health
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Female. * 40-55 years of age. * Must be in good general health. * Must have concerns with overall skin health and appearance, including: Fine lines and wrinkles The appearance of dark spots * Must be using the same cleanser, toner, and moisturizer for at least one month prior to starting the study. * Must be willing to keep using the same cleanser, toner, and moisturizer for the duration of the study. * Must not be using oral or topical retinoids. * In the last three months, has not introduced any new medications or supplements that target skin health. * Must be willing to comply with the protocol.

Exclusion criteria

* Anyone with an allergy to bees or bee products. * Females who are pregnant or breastfeeding. * Unwilling to follow the protocol. * Unwilling to maintain use of the same cleaner, toner, and moisturizer for the duration of the study. * Currently participating in another study. * Use of oral or topical retinoids. * Individuals with cystic acne or otherwise self-reported very acne-prone skin. * Use of a prescription medication relevant to the skin. * Anyone undergoing cosmetic procedures during the study, including Botox, laser, or chemical peel treatments. * Anyone sensitive or allergic to any ingredients found in the products. * Anyone with severe chronic conditions, including oncological conditions, psychiatric disorders, or diabetes.

Design outcomes

Primary

MeasureTime frameDescription
Changes in signs of skin health over time assessed via Optic Elite Skin Analysis. [Timeframe: Baseline to Week 8]8 weeksThe Optic Elite skin analysis system clinically measures the surface and subsurface layers of skin using digital imaging technology

Secondary

MeasureTime frameDescription
Changes in self-perceived skin clarity. [Timeframe: Baseline to Week 8]8 weeksMeasured via study-specific questionnaires using a 5-point Likert scale. A lower score indicates a more favourable response, with 0=Not noticeable and 4=Severe.
Changes in self-perceived skin hydration. [Timeframe: Baseline to Week 8]8 weeksMeasured via study-specific questionnaires using a 5-point Likert scale. A lower score indicates a more favourable response, with 0=Not noticeable and 4=Severe.
Changes in self-perceived skin texture. [Timeframe: Baseline to Week 8]8 weeksMeasured via study-specific questionnaires using a 5-point Likert scale. A lower score indicates a more favourable response, with 0=Not noticeable and 4=Severe.
Changes in self-perceived appearance of fine lines and wrinkles. [Timeframe: Baseline to Week 8]8 weeksMeasured via study-specific questionnaires using a 5-point Likert scale. A lower score indicates a more favourable response, with 0=Not noticeable and 4=Severe.
Changes in self-perceived skin irritation. [Timeframe: Baseline to Week 8]8 weeksMeasured via study-specific questionnaires using a 5-point Likert scale. A lower score indicates a more favourable response, with 0=Not noticeable and 4=Severe.
Changes in self-perceived skin brightness. [Timeframe: Baseline to Week 8]8 weeksMeasured via study-specific questionnaires using a 5-point Likert scale. A lower score indicates a more favourable response, with 0=Not noticeable and 4=Severe.
Changes in self-perceived skin tone evenness. [Timeframe: Baseline to Week 8]8 weeksMeasured via study-specific questionnaires using a 5-point Likert scale. A lower score indicates a more favourable response, with 0=Not noticeable and 4=Severe.
Changes in self-perceived skin hyperpigmentation. [Timeframe: Baseline to Week 8]8 weeksMeasured via study-specific questionnaires using a 5-point Likert scale. A lower score indicates a more favourable response, with 0=Not noticeable and 4=Severe.

Countries

United States

Outcome results

None listed

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