Test Participation

Application for Participation

[Recruiting] [26041-1] Efficacy test for lotion and emulsion with multiple races
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2026.01.19 13:44
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This test has been reviewed by the Dermapro Institute Bioethics Committee.

  • Test Name

    [26041-1] Efficacy test for lotion and emulsion with multiple races
  • Test Purpose

    To evaluate skin hydration, color, elasticity, pore, melanin, hyper-pigmentation and wrinkle effect for the test product on multiple races skin
  • Test Method

    -5 visits over an 8-week period
    -Approximately 90 minutes per visit
  • Test Period

    2026-01-26~2026-03-27
  • Test location and person in charge

    Head Office (Bangbae-dong), Basement Level 1 (B1) / Anti-Aging Team, Researcher Eunjoo Kin (Tel: 02-597-5415)
  • Number of people recruited

    20
  • recruited Period

    2026-01-19~2026-02-06
  • Visit schedule

    1st Visit (Before use): January 26, 2026 / January 27, 2026 2nd Visit (3 days after use): January 29, 2026 / January 30, 2026 3rd Visit (7 days after use): February 2, 2026 / February 3, 2026 4th Visit (4 weeks after use): February 23, 2026 ~ February 27, 2026 5th Visit (8 weeks after use): March 23, 2026 ~ March 27, 2026
  • Selection criteria

    Female or male participants with facial wrinkles and pigmentation
    Female or male participants aged 30 years or older
  • Exclusion criteria

    -Subjects who are pregnant, nursing condition or planning to become pregnant
    -Subjects who treat immune-suppressant within one month
    -Subjects who participate in a previous study without an appropriate intervening period (2 weeks) between studies
    -Subjects who have sensitive or hypersensitive skin
    -Subjects who have damaged skin in, or around the test site, which includes sunburn, tattoos, scars or other disfiguration on the test site
    -Subjects who use of similar treatment related to the study during the previous three months
    -Subjects who have an experience on the test site (skin decortications, Botox and other skin treatment)
    -Subjects who have chronic disease (diabetes, asthma, high blood-pressure)
    -Subjects who have atopic dermatitis
    -Subjects who took any oral or topical drug for the intension of whitening during recent 6 months
    -Subjects who use whitening and anti-wrinkle treatment during the previous two weeks
    -Subjects who routinely use products containing kojic acid or whitening product
    -Subjects who use eye drops during the previous 1 week
    -Subjects who use cream products starting two weeks prior to study initiation
    -Subjects who have problem which may interfere with the aim of the study as the judgment of the investigator
  • Examination participation fee

    200 Thousnad KRW
  • precautions

    This page is for application only.


    Your participation will be confirmed only after you receive a phone call or text message from the assigned researcher.

    During the designated period prior to participation, the use of eye drops, artificial tears, exfoliating pads, or toner pads is not allowed.
    (If any traces of such products are visible in photographs, the applicant may be excluded from the study.)

  • Predictable side effects

    During or after the study, adverse reactions may occur at the test site, including redness accompanied by stinging, burning, or itching sensations, as well as swelling, papules, or vesicles.
  • Inquiry about subject's rights
    and interests

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