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Age-related Changes in Skin Appearance and PhysiologyBCP-SkinNCT07516756

Effect of Collagen Peptides on Skin Health: A Clinical Trial

A study testing Specific Collagen Peptides in people with Age-related Changes in Skin Appearance and Physiology, run by Collagen Research Institute at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this clinical trial is to evaluate whether daily oral supplementation with 2.5 g of specific bioactive collagen peptides (SCP) can improve skin physiology in healthy adult women aged 35-55 years. Read more about this study

Who is it for?
Ages 35 to 55 years, women onlyHealthy volunteers can take part
What is being tested?
Specific Collagen Peptides
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
66 participants
Where
1 siteChina
Study dates
8 Aug 2024to 4 Oct 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 35 to 55 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Fitzpatrick skin type III-IV
  • Presence of crow's feet wrinkles graded 2-4
  • Presence of under-eye fine lines graded 2-5
  • Generally in good health
  • Able to comply with study procedures and visit schedule

Who cannot join

  • Use of systemic or topical anti-inflammatory medication, including corticosteroids, within the 4 weeks prior to baseline
  • Known hypersensitivity or allergy to any ingredient of the investigational products
  • Pregnancy, breastfeeding, or intention to become pregnant during the study period
  • History of relevant dermatological conditions: psoriasis, eczema, atopic dermatitis, or severe acne
  • Presence of birthmarks, hyperpigmentation, active inflammation, or other visible skin abnormalities in the test areas
  • Recent aesthetic procedures Use of anti-aging or topical treatments
Show all 13Show fewer
  • Intake of nutritional supplements
  • Participation in other clinical studies within the past 2 months
  • Significant lifestyle or dietary changes during the study period
  • Excessive UV exposure
  • Systemic diseases, including heart, immune, vascular, liver, gallbladder, or kidney disorders
  • Known allergies to foods, cosmetics, skincare products, or topical medications
  • Any other condition that, in the investigator's opinion, would make the participant ineligible

Trial locations and contacts

1 site in 1 country.

China1 site
  • Beijing EWISH Testing Technology Co., Ltd

    Beijing, Haidan, 100142

Other trials in China

About this study

Official title: Impact of Oral Supplementation of Specific Bioactive Collagen Peptides on Human Skin Physiology: A Randomized, Double-Blind, Placebo-Controlled Trial

The goal of this clinical trial is to evaluate whether daily oral supplementation with 2.5 g of specific bioactive collagen peptides (SCP) can improve skin physiology in healthy adult women aged 35-55 years. The main questions it aims to answer are:

Does SCP supplementation increase skin hydration and barrier function? Does SCP improve skin elasticity, firmness, and collagen content? Does SCP reduce the appearance of periorbital wrinkles and improve overall skin appearance? Researchers will compare SCP supplementation to a placebo (a look-alike substance containing no collagen peptides) to see if SCP supports skin structure and appearance over eight weeks.

Read more

Participants will:

Consume one sachet of SCP or placebo daily for eight weeks Attend three study visits at baseline, week 4, and week 8 for facial imaging, instrumental skin measurements, and expert assessments Have objective measures taken, including skin hydration, transepidermal water loss, elasticity, firmness, dermal collagen content, and 3D wrinkle morphology Complete subjective skin assessments rated by trained evaluators using a visual analogue scale Report any adverse events or intolerance reactions at each visit This study is designed to provide an integrated evaluation of multiple skin parameters, including barrier function, biomechanical properties, dermal matrix composition, and wrinkle characteristics, in a single trial. By combining objective and subjective measures, the study aims to generate robust and clinically interpretable evidence for the effects of oral collagen peptide supplementation on skin health.

Read the detailed description

This clinical trial investigates whether daily oral supplementation with specific bioactive collagen peptides (SCP) can support healthy skin in adult women. Skin aging is a natural process influenced by genetics, hormones, and lifestyle, leading to wrinkles, reduced elasticity, and changes in skin structure. Collagen is a key protein that helps maintain skin strength and elasticity, and its levels decline with age.

The study will evaluate the effects of an 8-week course of SCP supplementation compared to a placebo in healthy women aged 35-55 years. Researchers aim to determine whether oral collagen peptides can improve skin hydration, elasticity, firmness, and overall appearance. This trial combines multiple objective and subjective measures to provide a comprehensive assessment of skin health, offering insights into non-invasive nutritional strategies to maintain skin structure and appearance over time.

The findings from this study are expected to enhance understanding of how collagen peptides affect skin physiology and contribute to evidence-based recommendations for supporting healthy skin.

Being tested
Placebo, Specific Collagen Peptides
Keywords
Bioactive collagen peptides, Oral supplementation, Skin aging, Skin hydration, Skin elasticity, Skin firmness, Wrinkles / periorbital wrinkles, Dermal extracellular matrix, Skin barrier function, Skin physiology, Healthy adult women, Randomized controlled trial (

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PlaceboDietary supplement

    Participants in this arm receive a matching placebo sachet once daily for 8 weeks. The placebo contains plant-derived maltodextrin and is identical in appearance, taste, and texture to the collagen peptide supplement. It is dissolved in warm water and consumed orally. Participants continue their usual lifestyle habits while taking the placebo.

  • Specific Collagen PeptidesDietary supplement

    Participants in this arm receive 2.5 g of specific bioactive collagen peptides (VERISOL®) once daily for 8 weeks. The powder is dissolved in warm water and consumed orally. The supplement contains defined collagen peptides derived from bovine type I collagen, which have been shown to support skin hydration, elasticity, firmness, dermal collagen content, and wrinkle reduction. Participants continue their usual lifestyle habits while taking the supplement.

Study groups in NCT07516756
Study groupRoleWhat they receive
Specific Collagen PeptidesExperimentalParticipants in this arm receive 2.5 g of specific bioactive collagen peptides (VERISOL®) once daily for 8 weeks. The powder is dissolved in warm water and consumed orally. The supplement contains defined collagen peptides derived from bovine type I collagen, which have been shown to support skin hydration, elasticity, firmness, dermal collagen content, and wrinkle reduction. Participants continue their usual lifestyle habits while taking the supplement.
Receives: Dietary Supplement: Specific Collagen Peptides
MaltodextrinPlacebo comparatorParticipants in this arm receive a matching placebo sachet once daily for 8 weeks. The placebo contains plant-derived maltodextrin and is identical in appearance, taste, and texture to the collagen peptide supplement. It is dissolved in warm water and consumed orally. Participants continue their usual lifestyle habits while taking the placebo.
Receives: Dietary Supplement: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. stratum corneum hydration (SCH)

    Stratum corneum hydration (SCH) measures the water content in the outermost layer of the skin, reflecting the skin's ability to retain moisture and maintain a healthy barrier. In this study, SCH is the primary efficacy endpoint, used to compare the effect of daily oral supplementation with specific bioactive collagen peptides (SCP) versus placebo over an 8-week period.

    SCH is assessed using a Corneometer CM825 at the cheek. Each site is measured six times, and the mean value is used for analysis. Higher SCH values indicate better skin hydration, whereas lower values suggest dryness or impaired barrier function. Changes in SCH over time are compared between the treatment and placebo groups to evaluate the impact of collagen peptide supplementation on skin hydration.

    Measured: From enrollment to the end of treatment at 8 weeks

Secondary outcomes (5)
  1. Transepidermal Water Loss (TEWL)

    TEWL measures the rate of water loss through the skin, indicating the integrity of the skin barrier. In this study, TEWL is assessed using the Tewameter TM 300 at the cheek in triplicate, with mean values used for analysis. Higher TEWL values suggest impaired barrier function, while lower values indicate better barrier integrity. Changes over the 8-week supplementation period are compared between the collagen peptide and placebo groups.

    Measured: From enrollment to the end of treatment at 8 weeks

  2. Skin Elasticity (R2 and R5) and Firmness (F4)

    Skin elasticity and firmness are evaluated using the Cutometer MPA580, which applies controlled suction to assess the biomechanical properties of the cheek.

    R2 (gross elasticity): overall skin elasticity R5 (net elasticity): elastic recovery relative to total deformation F4 (firmness): resistance to deformation Measurements are performed in triplicate and averaged. These parameters provide insight into the skin's structural resilience and are compared between treatment and placebo groups over 8 weeks.

    Measured: From enrollment to the end of treatment at 8 weeks

  3. Dermal collagen content

    Dermal collagen content is measured non-invasively using the SIAMETRICS SIAscope V at a 2 mm depth of the cheek. This device quantifies dermal chromophores, including collagen, to assess the integrity and composition of the dermal extracellular matrix. Changes over the 8-week intervention are compared between the SCP and placebo groups.

    Measured: From enrollment to the end of treatment at 8 weeks

  4. Wrinkle Morphology

    Wrinkle characteristics around the eyes (area, volume, depth) are measured using the Derma TOP 3D imaging system.

    Measured: From enrollment to the end of treatment at 8 weeks

  5. Skin Appearance (3D Imaging + VAS)

    Full-face 2D images are captured with VISIA-CR for additional objective assessments, including spots, skin tone, hydration, and elasticity.

    Subjective evaluations are performed using a Visual Analogue Scale (VAS) by three trained evaluators, assessing:

    Smoothness Glossiness Fineness Elasticity Crow's feet and under-eye fine lines VAS scores range from 0 to 10. Higher values indicate better outcomes for attributes such as smoothness, elasticity, and glossiness, while lower values reflect improvement in periorbital wrinkles. Changes over the 8-week supplementation period are compared between treatment and placebo groups.

    Measured: From enrollment to the end of treatment at 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Apr 2026
  2. Study start8 Aug 2024
  3. Primary completion4 Oct 2024
  4. Study completion4 Oct 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
66 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07516756
Sponsor's protocol ID
SECCR2024-97-01
Acronym
BCP-Skin
Status last verified
Apr 2026
First submitted
1 Apr 2026
Last updated
8 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request. The data will not be publicly available due to privacy and ethical restrictions.

Publications

  • Vollmer DL, West VA, Lephart ED. Enhancing Skin Health: By Oral Administration of Natural Compounds and Minerals with Implications to the Dermal Microbiome. Int J Mol Sci. 2018 Oct 7;19(10):3059. doi: 10.3390/ijms19103059.

    PubMed 30301271
  • Dahnhardt D, Dahnhardt-Pfeiffer S, Segger D, Poeggeler B, Lemmnitz G. Restoration of the Ultrastructural Integrity of the Dermal Collagen Network by 12-Week Ingestion of Special Collagen Peptides. Dermatol Ther (Heidelb). 2024 Sep;14(9):2509-2521. doi: 10.1007/s13555-024-01251-8. Epub 2024 Aug 16.

    PubMed 39150674
  • Lin P, Alexander RA, Liang CH, Liu C, Lin YH, Lin YH, Chan LP, Kuan CM. Collagen formula with Djulis for improvement of skin hydration, brightness, texture, crow's feet, and collagen content: A double-blind, randomized, placebo-controlled trial. J Cosmet Dermatol. 2021 Jan;20(1):188-194. doi: 10.1111/jocd.13500. Epub 2020 Jun 12.

    PubMed 32530124
  • Inacio PAQ, Chaluppe FA, Aguiar GF, Coelho CF, Vieira RP. Effects of Hydrolyzed Collagen as a Dietary Supplement on Fibroblast Activation: A Systematic Review. Nutrients. 2024 May 21;16(11):1543. doi: 10.3390/nu16111543.

    PubMed 38892477
  • Dierckx S, Patrizi M, Merino M, Gonzalez S, Mullor JL, Nergiz-Unal R. Collagen peptides affect collagen synthesis and the expression of collagen, elastin, and versican genes in cultured human dermal fibroblasts. Front Med (Lausanne). 2024 May 1;11:1397517. doi: 10.3389/fmed.2024.1397517. eCollection 2024.

    PubMed 38751975
  • Fu Y, Young JF, Rasmussen MK, Dalsgaard TK, Lametsch R, Aluko RE, Therkildsen M. Angiotensin I-converting enzyme-inhibitory peptides from bovine collagen: insights into inhibitory mechanism and transepithelial transport. Food Res Int. 2016 Nov;89(Pt 1):373-381. doi: 10.1016/j.foodres.2016.08.037. Epub 2016 Aug 28.

    PubMed 28460927
  • Feng M, Betti M. Transepithelial transport efficiency of bovine collagen hydrolysates in a human Caco-2 cell line model. Food Chem. 2017 Jun 1;224:242-250. doi: 10.1016/j.foodchem.2016.12.044. Epub 2016 Dec 18.

    PubMed 28159262
  • Osawa Y, Mizushige T, Jinno S, Sugihara F, Inoue N, Tanaka H, Kabuyama Y. Absorption and metabolism of orally administered collagen hydrolysates evaluated by the vascularly perfused rat intestine and liver in situ. Biomed Res. 2018;39(1):1-11. doi: 10.2220/biomedres.39.1.

    PubMed 29467346
  • Liu Z, Li Y, Song H, He J, Li G, Zheng Y, Li B. Collagen peptides promote photoaging skin cell repair by activating the TGF-beta/Smad pathway and depressing collagen degradation. Food Funct. 2019 Sep 1;10(9):6121-6134. doi: 10.1039/c9fo00610a. Epub 2019 Sep 9.

    PubMed 31497829
  • Wang L, Zhang Y, Zhu Z, Zheng F, Gao R. Food-derived collagen peptides: safety, metabolism, and anti-skin-aging effects. Current Opinion in Food Science. 2023;51:101012. https://doi.org/10.1016/j.cofs.2023.101012.

  • He X, Gao X, Guo Y, Xie W. Research Progress on Bioactive Factors against Skin Aging. Int J Mol Sci. 2024 Mar 28;25(7):3797. doi: 10.3390/ijms25073797.

    PubMed 38612608
  • Yang Q, Li H, Zhang H, Ma L, Zhang X, Wu J. Effectiveness of dietary supplements for skin photoaging in healthy adults: a systematic review and meta-analysis of randomized controlled trials. Front Med (Lausanne). 2025 Jul 21;12:1582946. doi: 10.3389/fmed.2025.1582946. eCollection 2025.

    PubMed 40761858
  • Michelotti A, Cestone E, De Ponti I, Pisati M, Sparta E, Tursi F. Oral intake of a new full-spectrum hyaluronan improves skin profilometry and ageing: a randomized, double-blind, placebo-controlled clinical trial. Eur J Dermatol. 2021 Dec 1;31(6):798-805. doi: 10.1684/ejd.2021.4176.

    PubMed 34933842
  • Morgado-Carrasco D, Gil-Lianes J, Jourdain E, Piquero-Casals J. Oral Supplementation and Systemic Drugs for Skin Aging: A Narrative Review. Actas Dermosifiliogr. 2023 Feb;114(2):114-124. doi: 10.1016/j.ad.2022.09.014. Epub 2022 Oct 4. English, Spanish.

    PubMed 36206809
  • Czajka A, Kania EM, Genovese L, Corbo A, Merone G, Luci C, Sibilla S. Daily oral supplementation with collagen peptides combined with vitamins and other bioactive compounds improves skin elasticity and has a beneficial effect on joint and general wellbeing. Nutr Res. 2018 Sep;57:97-108. doi: 10.1016/j.nutres.2018.06.001. Epub 2018 Jun 9.

    PubMed 30122200

Questions about this trial

What is this clinical trial studying?

A study testing Specific Collagen Peptides in people with Age-related Changes in Skin Appearance and Physiology, run by Collagen Research Institute at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

stratum corneum hydration (SCH) (time frame: From enrollment to the end of treatment at 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07516756, which also lists 36 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Apr 2026.

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