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CompletedNCT06847035Updated Feb 28, 2025

Efficacy Study of Oral Collagen Peptide on Skin Condition Improvement

An interventional study of Active Comparator and Placebo Comparator in Skin Aging, sponsored by Shanghai Meifute Biotechnology Co., Ltd. Completed at 1 site in China. Open to female participants aged 35 Years to 55 Years. Per ClinicalTrials.gov, last updated 2025-02-28.

Sponsored by Shanghai Meifute Biotechnology Co., Ltd · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Jul 2024, registered Feb 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
35 Years to 55 Years
Sex
Female
01

Study summary

To assess if oral intake of collagen peptide can improve skin conditions such as skin thickness, density and firmness.

Read the detailed description

This is an one site, randomized, double-blind controlled clinical trial to assess the oral supplement of LISAVEI collagen peptide solid beverage on skin ageing improvement. Study product with collagen peptide and placebo product without collagen were randomly assigned to 90 eligible participants enrolled according to the inclusion and exclusion criteria. They took the assigned product once daily dissolved in 100 ml warm water for 12 weeks with 4-week regression phase(without intake of the test products), and visit the study site in Shanghai for four times(before starting the treatment, after 8 and 12 weeks, and 4 weeks after the last intake). Skin measurements including skin firmness, skin density, skin hydration and skin barrier were carried out at each visit with professional equipment and imaging system. Data were analyzed to validate if the administration of the test collagen peptide solid beverage will improve skin aging parameters such as firmness, thickness, density, hydration and skin barrier compared to placebo. The lasting effect was also observed by comparing between the two groups after 4-week regression time.

02

Conditions studied

  • Skin Aging

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03

In context

Skin Diseases

538 studies on the registry are indexed under Skin Diseases; 92 are open to participants now.

This study's enrollment of 90 is above the median of 60 across 372 interventional studies indexed under Skin Diseases.

Browse Skin Diseases studies →

Lead sponsor

This is the only study on the registry with Shanghai Meifute Biotechnology Co., Ltd as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 55 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  1. Healthy female adults aged between 35-55 years old
  2. With fine wrinkles and skin laxity
  3. Personal informed consents to participate in the study
  4. Agree to keep their daily skincare routine unchanged for the duration of the study
  5. Maintain good sun protection habits
  1. Agree to refrain from wearing make-up on the face on the each study visit

Exclusion criteria

Exclusion Criteria

  1. Female who is pregnant or nursing or planning to become pregnant during the course of the study
  2. Individuals who are in the perimenopausal stage.
  3. BMI\<18.5 or BMI >27.9
  4. Individuals suffering from chronic systemic diseases such as cardiovascular, cerebrovascular, liver, and kidney diseases.
  5. Individuals who have diabetes.
  6. Individuals suffering from skin conditions such as psoriasis, eczema, atopic dermatitis, and severe acne.
  7. Individuals with depression or sleep disorders, those who smoke, and those who abuse alcohol.
  8. Individuals who are using hormonal drugs, medications for obesity, absorption inhibitors, antidepressants, or appetite suppressants.
  9. Individuals who have used hormones or anti-inflammatory drugs on their face and upper arms within the past two months.
  10. Individuals who received facial laser therapy, chemical peeling or UV overexposure in the past 3 months
  11. Individuals who can not avoid prolonged exposure to sunlight.
  12. Individuals who are currently participating in other clinical studies or trials.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
90 participants (actual)

Study arms

  • Active comparator
    Active Comparator

    collagen peptide solid beverage

    Dietary Supplement: Active Comparator

  • Placebo comparator
    Placebo Comaprator

    placebo solid beverage

    Dietary Supplement: Placebo Comparator

Interventions

  • Dietary supplementActive Comparator

    LISAVEI collagen peptide solid beverage ( contain 5 g collagen peptide),once daily for 12 weeks

  • Dietary supplementPlacebo Comparator

    placebo solid beverage (Maltodextrin with edible flavor),once daily for 12 weeks

    Also known as: placebo solid beverage

06

What researchers measure

Primary outcomes

  1. Skin firmness

    The changes of skin firmness parameter tested by Cutometer MPA580

    Time frame: before product treatment (T 0), after 8 weeks(T 1)and 12 weeks(T 2) of daily product intake, 4 weeks after the last intake(T 3, 4-week regression phase)

  2. Skin thickness

    The changes of skin thickness (μm) tested by Ultrascan UC 22

    Time frame: before product treatment (T 0), after 8 weeks(T 1)and 12 weeks(T 2) of daily product intake, 4 weeks after the last intake(T 3, 4-week regression phase)

  3. Skin density

    The changes of skin density tested by Ultrascan UC 22

    Time frame: before product treatment (T 0), after 8 weeks(T 1)and 12 weeks(T 2) of daily product intake, 4 weeks after the last intake(T 3, 4-week regression phase)

Secondary outcomes

  1. Skin hydration

    The changes of skin hydration tested by Corneometer CM825

    Time frame: before product treatment (T 0), after 8 weeks(T 1)and 12 weeks(T 2) of daily product intake, 4 weeks after the last intake(T 3, 4-week regression phase)

  2. Skin barrier

    The changes of Trans Epidermal Water Loss (skin barrier parameter) tested by Tewameter TM300

    Time frame: before product treatment (T 0), after 8 weeks(T 1)and 12 weeks(T 2) of daily product intake, 4 weeks after the last intake(T 3, 4-week regression phase)

  3. Facial image

    Photo documents of left, right and frontal facial views

    Time frame: before product treatment (T 0), after 8 weeks(T 1)and 12 weeks(T 2) of daily product intake, 4 weeks after the last intake(T 3, 4-week regression phase)

07

Study locations

1 site
  • Shanghai Fumei Dermatology Clinic
    Shanghai, Shanghai 021, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 28, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06847035
Lead sponsor
Shanghai Meifute Biotechnology Co., Ltd
Responsible party
Sponsor
First posted
Feb 26, 2025
Start date
Jul 25, 2024
Primary completion
Nov 19, 2024
Completion
Nov 19, 2024
Last update
Feb 28, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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