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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06148740
Other study ID # 20376
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 9, 2023
Est. completion date February 28, 2024

Study information

Verified date November 2023
Source Manuka Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a virtual, single-group clinical trial that will last 8 weeks. Participants will use the Manuka Health Pro Vitality Daily Restorative Face Serum with Propolis & Vitamin C 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date February 28, 2024
Est. primary completion date February 28, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 30 Years to 42 Years
Eligibility Inclusion Criteria: - Female between 30-42 years of age. - Must be in good general health. - Must have concerns with overall skin health and appearance, including: Spots or blemishes Uneven skin tone Dull-looking skin - 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Manuka Health Pro Vitality Daily Restorative Face Serum with Propolis & Vitamin C
Skin serum containing propolis, vitamin C, and manuka honey.

Locations

Country Name City State
United States Citruslabs Santa Monica California

Sponsors (2)

Lead Sponsor Collaborator
Manuka Health Citruslabs

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in signs of skin health over time assessed via Optic Elite Skin Analysis. [Timeframe: Baseline to Week 8] The Optic Elite skin analysis system clinically measures the surface and subsurface layers of skin using digital imaging technology. Participants will receive a score that can be compared between time points. 8 weeks
Secondary Changes in self-perceived skin clarity. [Timeframe: Baseline to Week 8] Measured 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. 8 weeks
Secondary Changes in self-perceived skin hydration. [Timeframe: Baseline to Week 8] Measured 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. 8 weeks
Secondary Changes in self-perceived skin texture. [Timeframe: Baseline to Week 8] Measured 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. 8 weeks
Secondary Changes in self-perceived skin pigmentation. [Timeframe: Baseline to Week 8] Measured 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. 8 weeks
Secondary Changes in self-perceived skin irritation. [Timeframe: Baseline to Week 8] Measured 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. 8 weeks
Secondary Changes in self-perceived skin brightness.[Timeframe: Baseline to Week 8] Measured 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. 8 weeks
Secondary Changes in self-perceived skin tone evenness. [Timeframe: Baseline to Week 8] Measured 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. 8 weeks
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