Clinical Trial to Evaluate the Efficacy of Skin Products to Improve Skin Quality and Health

February 25, 2025 updated by: Truology

A Clinical Trial to Evaluate the Efficacy of Skin Products to Improve Skin Quality and Health

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.

Study Overview

Study Type

Interventional

Enrollment (Actual)

33

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Nevada
      • Las Vegas, Nevada, United States, 89118
        • Citruslabs

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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
  • Anyone with any known allergies or hypersensitivities to any of the study product ingredients:

Truology A2 - Water, Glycerin, Pentylene Glycol, Niacinamide, Cyclodextrin, Polysorbate 20, Squalane, Coco-Caprylate/-Caprate, Cetearyl Alcohol, Cetyl Alcohol, Sodium Hyaluronate, Palmitoyl Tripeptide-5, Caprooyl Tetrapeptide-3, Hydroxyethylcellulose, Ceteareth-20, Beta Glucan, Resveratrol, Dimethyl Sulfone, Retinal, Tocopherol, Tetrahexyldecyl Ascorbate, Dextran, Dipalmitoyl Hydroxyproline, Lactic Acid, Arnica Montana Flower Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Camellia Sinensis (Green Tea) Leaf Extract, Salix Nigra (Willow) Bark Extract, Epilobium Angustifolium Flower/Leaf/Stem Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Lonicera Caprifolium (Honeysuckle) Flower Extract, Rubus Chamaemorus Seed Oil, Sclerotium Gum, Phenoxyethanol, Ethylhexylglycerin, Titanium Dioxide.

C-Boost - Water, Tetrahexyldecyl Ascorbate, Squalane, Glycerin, Propanediol, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Sodium Hyaluronate, Trifluoroacetyl Tripeptide-2, Astaxanthin, Bisabolol, Glutathione, Ergothioneine, Cetearyl Olivate, Sorbitan Olivate, Ceteareth- 20, Dextran, Ferulic Acid, Fulvic Acid, Plankton Extract, Chlorella Vulgaris Extract, Zingiber Officinale (Ginger) Root Extract, Camellia Sinensis (Green Tea) Leaf Extract, Vitis Vinifera (Grape) Seed Extract, Curcuma Longa (Turmeric) Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Arctostaphylos Uva-Ursi-Leaf (Bearberry) Extract, Tocopherol, Magnesium Ascorbyl Phosphate, Lecithin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Phenoxyethanol, Ethylhexylglycerin, Sodium Hydroxide.

Barrier Restore - *Organic Aloe Barbadensis Leaf Juice, Glycerin, Squalane, Caprylic/Capric Triglyceride, Linoleic Acid, Pentylene Glycol, Cetyl Alcohol, Coco-Caprylate/Caprate, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Fructooligosaccharides, Beta Vulgaris (Beet) Root Extract, Sodium Hyaluronate, Palmitoyl Tripeptide-38, Palmitoyl Tripeptide-5, Palmitoyl Dipeptide-5 Diaminobutyroyl Hydroxythreonine, Palmitoyl Hexapeptide-12, Ceramide Ng, Bisabolol, Tocopherol, Tetrahexyldecyl Ascorbate, Dimethicone, Tetradecyl Aminobutyroylvalylaminobutyric Urea Trifluoroacetate, Tribehenin, Peg 10 Rapeseed Sterol, (Oat) Beta Glucan, Ceteareth-20, Hydroxyethylcellulose, Cetearyl Olivate, Sorbitan Olivate, Hydroxypropyl Cyclodextrin, Cassia Angustifolia Seed Polysaccharide, Linolenic Acid, Tremella Fuciformis Sporocarp Extract, Sarcothalia Circumcincta Extract, Opuntia Ficus-Indica (Nopal Cactus) Extract, Saccharomyces Cerevisiae (Yeast) Extract, Cyathea Medullaris Leaf Extract, Opuntia Streptacantha Stem Extract, Symphytum Officinale (Comfrey) Rhizome/Root Extract, Lycium Chinense (Goji Berry) Extract, Hippophae Rhamnoids (Seabuckthorn) Oil, Lactobacillus Ferment, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Disodium Edta, Carbomer, Phenoxyethanol, Ethylhexylglycerin, Sodium Hydroxide

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Truology Skincare Routine
A single-arm study in which all participants will use the Truology Skincare Routine for 6 weeks.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Improvement in self-reported skin health symptoms (measured via questionnaires)
Time Frame: Baseline, Day 1, Week 2, Week 4, Week 6
Baseline, Day 1, Week 2, Week 4, Week 6

Secondary Outcome Measures

Outcome Measure
Time Frame
Changes in overall facial skin quality and health (measured via expert skin grading)
Time Frame: Baseline and Week 6
Baseline and Week 6

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Collaborators

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 21, 2024

Primary Completion (Actual)

January 10, 2025

Study Completion (Actual)

January 10, 2025

Study Registration Dates

First Submitted

February 25, 2025

First Submitted That Met QC Criteria

February 25, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 25, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 20455

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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