Ovolux Beauty From Within Trial#2

NCT07188051 | Enrolling By Invitation

• 1 other identifier: STNCLI1Q
• Study Type: interventional
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to evaluate the effectiveness of an eggshell membrane dietary supplement (Ovolux brand) in supporting beauty from within.

Conditions

Skin Sagging; Skin Wrinkling; Skin Dryness

Keywords

ovolux; eggshell membrane; beauty; skin elasticity; wrinkles; hair; fingernails

Outcome Measures

Primary Outcomes (1)

• Change in Skin Elasticity

  Measurement of facial skin elasticity parameters (R0, R2, R5, R6 and R9) via Cutometer® to determine if it improves or worsens

  Baseline, Week 4, Week 8, and Week 12

Secondary Outcomes (4)

• Change in Skin Hydration

  Baseline, Week 4, Week 8, and Week 12

• Change in Hair Thickness/Density

  Baseline, Week 12

• Change in Skin Wrinkles

  Baseline and Week 12

• Participant Self-Assessment Questionnaires

  Baseline, Week 4, Week 8, and Week 12

Study Arms (2)

Active

EXPERIMENTAL

Active intervention (Ovolux)

Dietary Supplement: Ovolux brand eggshell membrane powder

Placebo

PLACEBO COMPARATOR

Placebo

Dietary Supplement: Placebo

Interventions

Ovolux brand eggshell membrane powder DIETARY_SUPPLEMENT

Unhydrolyzed eggshell membrane powder

Active

Placebo DIETARY_SUPPLEMENT

psyllium husk fiber powder

Placebo

Eligibility Criteria

• Age: 35 Years - 65 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Participant is willing and able to read, understand, and provide written Informed Consent and Photo Release.
• Participant is a healthy female or male, aged 35 through 65 years (inclusive).
• Participant is willing and able to swallow capsules.
• Participant has self-perceived facial wrinkles and facial sagging skin.
• Participant is seeking improvements to hair and nails such as hair growth and thickness and nail strength and appearance.
• Participant agrees to keep their hair at least 3 inches long.
• Participant is willing to comply with all study procedures and attend all study visits.
• Participant agrees not to have any hair cosmetic procedures such as relaxers or perms, etc. while on the study. Coloring/dyeing is permitted if part of the participant's regular routine and this routine is maintained during the study.
• Participant is willing to forego taking any hair, nail or skin supplements or using/applying any other hair, nail or skin products on their hair/scalp, nails or face that promote nail or hair growth or are collagen boosting for the duration of the study.
• Participant is willing to discontinue any hair or nail or collagen boosting dietary or nutritional supplements two weeks before the onset of the study and for the study duration. Dietary supplements such as a general multi-vitamin, vitamins A, C or D, iron or calcium are acceptable.
• Participant agrees not to wet their face or consume hot or cold or caffeine containing foods or beverages within 2 hours of all visits.
• Participant reviewed the ingredient list for the test article (dietary supplement) and the placebo and, to the best of their knowledge, confirmed they have no sensitivity or allergy to the ingredients.
• Females of child bearing potential must agree to use an adequate method of birth control, which include: systemic birth control (must have been on the same type of systemic birth control for at least 3 months prior starting the study and must not change the type of birth control during the study); diaphragm with spermicide, condom with spermicide; IUD (hormonal or copper); Vasectomized partner; bilateral tubal ligation; or Abstinence. Females who are post-menopausal (absence of menses for at least 1 year), have had a hysterectomy or have had a bilateral oophorectomy do not need any additional birth control are considered to be not of childbearing potential; (Confirmed by verbal response only).

You may not qualify if:

• Participant is allergic to eggs or egg proteins.
• Participant is a smoker.
• Participant has a current skin disease on or near the scalp (e.g., eczema, psoriasis) or anywhere else on the body.
• Participant has any allergies or sensitivities to any dietary or nutritional supplements or their ingredients.
• Participant has artificial nails (press-on, glue-on, gel, acrylic, etc.). Nail polish is permitted if part of regular nail routine and if this routine is maintained during the study.
• Participation in another supplement study in the past 30 days.
• Participant has dreads or weaves.
• Participant has had any chemical hair procedure (used relaxers, perms, etc.) in the last 8 weeks.
• Participant has dyed their hair within the last 3 days.
• Participant has a diagnosed hair loss disorder such as alopecia areata, scarring alopecia, and/or androgenetic alopecia and/or pattern baldness.
• Participant is taking or using any medications or supplements (over the counter or prescription, topical or oral) for hair growth such as minoxidil, finasteride, dutasteride, spironolactone, collagen, amino acids, keratin, biotin, rosemary oil, corticosteroid injections, etc. or treatments for hair growth such as laser treatment or supplements for nails or skin.
• Participant is under treatment by a medical professional for a hair/scalp, nail or skin condition.
• Participant has any concomitant skin diseases of the scalp or skin such as atopic dermatitis, seborrheic dermatitis, psoriasis, eczema, tinea capitis, etc. or irritation such as rash, sores, etc. on the scalp.
• Participant has an infestation on the scalp such as lice.
• Female Only: Participant is pregnant, planning to become pregnant during the course of the study or nursing (self-reported).

Sponsors & Collaborators

• Princeton Consumer Research Corporation: collaborator
• ESM Technologies, LLC: lead

Study Sites (1)

Princeton Consumer Research Corp.

Cincinnati, Ohio, 45239, United States

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Single-center, randomized, double-blinded, placebo controlled design

Study Record Dates

• First Submitted: September 10, 2025
• First Posted: September 23, 2025
• Study Start: September 22, 2025
• Primary Completion: January 31, 2026
• Study Completion: February 25, 2026
• Last Updated: December 18, 2025

Record last verified: 2025-12

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)