Clinical Trial to Evaluate the Efficacy of Skin Products to Improve Skin Quality and Health
A Clinical Trial to Evaluate the Efficacy of Skin Products to Improve Skin Quality and Health
1 other identifier
interventional
33
1 country
1
Brief Summary
This clinical trial evaluates the efficacy of three skincare products-Truology A2 (0.2% Retinaldehyde Serum), Truology C-Boost, and Truology Barrier Restore-in improving skin quality and health. The study will assess improvements in skin firmness, evenness, brightness, hydration, fine lines/wrinkles, redness, and skin stress/irritation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 21, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 10, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 10, 2025
CompletedFirst Submitted
Initial submission to the registry
February 25, 2025
CompletedFirst Posted
Study publicly available on registry
March 3, 2025
CompletedMarch 3, 2025
February 1, 2025
3 months
February 25, 2025
February 25, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Improvement in self-reported skin health symptoms (measured via questionnaires)
Baseline, Day 1, Week 2, Week 4, Week 6
Secondary Outcomes (1)
Changes in overall facial skin quality and health (measured via expert skin grading)
Baseline and Week 6
Study Arms (1)
Truology Skincare Routine
EXPERIMENTALA single-arm study in which all participants will use the Truology Skincare Routine for 6 weeks.
Interventions
Truology A2 (0.2% Retinaldehyde Serum) - Applied once daily at night after cleansing.
Truology C-Boost - Applied twice daily (morning \& night).
Applied twice daily (morning \& night) as the final skincare step.
Eligibility Criteria
You may qualify if:
- Be female-at-birth
- Be aged 35-55
- Anyone currently experiencing issues with skin health, including: Poor skin texture, Skin discoloration, Appearance of fine lines and wrinkles Dull skin, Poor skin firmness, Dry skin, Skin redness, Irritated and stressed skin
- Willing to use the test products as follows: Truology A2 - Once a day at night. Use 1 pump for the whole face. Use first after cleansing the skin on dry skin. C-Boost - Twice a day (AM \& PM). In the morning, first use one pump for the full face after cleansing the skin. At night, use the A2 first, then C-Boost. Barrier Restore - Twice a day (AM \& PM). Use one pump for the full face. Use it after C-Boost for the final step in the skincare routine, and complete questionnaires and take photos
- Have been using the same skincare routine for at least one month prior to the study, i.e., cleanser, toner, and make-up remover
- Willing to maintain the same skincare routine and products throughout the 6-week trial, e.g., moisturizer, cleanser, or SPF
- Have been consistently taking medications, oral supplements, or herbal remedies targeted at skin health and appearance for at least 3 months prior to the study and willing to maintain this routine for the duration of the study
- Agree to avoid using any other products or new forms of regular medication or supplements that target skin health and appearance
- Anyone who is generally healthy - does not live with any uncontrolled chronic disease
- Anyone who is currently using or has used the past, exfoliating acids (AHAs/BHA) or retinoids in (i.e., salicylic acid, glycolic acid, mandelic acid, or lactic acid).
- Anyone willing to stop using exfoliating acids or retinoids for the duration of the study
- Anyone in good general health
- Anyone who resides in the United States
You may not qualify if:
- Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders
- Anyone currently using a prescription skin treatment
- Anyone with known severe allergic reactions
- Anyone unwilling to avoid excessive sun exposure
- Any women who are pregnant, breastfeeding, or attempting to conceive
- Anyone unwilling to follow the study protocol
- Anyone who identifies as having sensitive skin
- Anyone who has undergone any facial surgeries or invasive skin treatments in the last 6 months
- Anyone who is planning to undergo any facial treatments during the study period, including botox, dermal filler, or chemical peels
- Anyone who has not stopped using hormonal birth control within the past month
- Anyone with any chronic skin conditions on the face (e.g., eczema or psoriasis)
- Anyone with a history of skin cancer or pre-cancerous skin lesions on the face
- Anyone currently testing, or plans to in the next 6 weeks, a product for another research study
- Anyone with a history of substance abuse
- Anyone who is currently, or has been for the past 3 months, a smoker
- +4 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Truologylead
- Citruslabscollaborator
Study Sites (1)
Citruslabs
Las Vegas, Nevada, 89118, United States
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 25, 2025
First Posted
March 3, 2025
Study Start
October 21, 2024
Primary Completion
January 10, 2025
Study Completion
January 10, 2025
Last Updated
March 3, 2025
Record last verified: 2025-02
Data Sharing
- IPD Sharing
- Will not share