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Effect of Oral Collagen Tripeptide on Skin Moisture and Wrinkles in Adult Women

Effect of Oral Collagen Tripeptide on Skin Moisture and Wrinkles in Adult Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03505684
Enrollment
84
Registered
2018-04-23
Start date
2017-12-24
Completion date
2018-07-30
Last updated
2018-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Skin Manifestations, Skin Wrinkling

Brief summary

Comparison of a randomized, double-blind, and control-group study for the effect of oral ingestion of collagen tripeptides derived from fish on dermal moistures and wrinkles body fat reduction in participants

Detailed description

The aim is to investigate the effect of oral ingestion of collagen tripeptides derived from fish on dermal moistures and wrinkles body fat reduction in participants by a randomized, double-blind, and control-group study.

Interventions

DIETARY_SUPPLEMENTCTP

1,000 mg of CTP was orally administered per day for 12 weeks.

DIETARY_SUPPLEMENTplacebo (starch)

placebo (starch)

Sponsors

Pusan National University Yangsan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

\- \> = 4 of Tewameter

Exclusion criteria

* Within the last 6 months, took skin surgery including cosmetic purpose * Diabetic patients with poor glycemic control with a fasting blood glucose of 160 mg/dl or more * Creatinine levels: more than twice the normal upper limit * AST (GOT) or ALT (GPT) levels: more than twice the normal upper limit * Uncontrolled hypertension * sun allergy or sensitive skin * functional cosmetics that affect dermal moistures and wrinkles within the last 3 months. * If you have participated or are planning to participate in another clinical trial within the past month * Alcohol abuser * If they are pregnant or lactating or have a pregnancy plan during the clinical trial Those with allergic reactions to the constituent food * Any person deemed inappropriate by the researcher for other reasons

Design outcomes

Primary

MeasureTime frameDescription
changes in Transepidermal Waterloss by Tewameterbaseline, after 6 weeks, and after 12 weekscomparison between baseline, after 6 weeks, and after 12 weeks

Secondary

MeasureTime frameDescription
changes in skin wrinkling indices by Visiometerbaseline, after 6 weeks, and after 12 weekscomparison between baseline, after 6 weeks, and after 12 weeks
skin elasticity by Cutometerbaseline, after 6 weeks, and after 12 weekscomparison between baseline, after 6 weeks, and after 12 weeks
changes in hydration level of the skin surface by Corneometerbaseline, after 6 weeks, and after 12 weekscomparison between baseline, after 6 weeks, and after 12 weeks

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026