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Human Application Test for Non-comedogenic Suitability of 'CureCode Soothing Relief Gel' on Acne-Prone Skin

Human Clinical Trial on Non-comedogenic Effect of CureCode Soothing Relief Gel

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011708
Enrollment
22
Registered
2026-03-11
Start date
2024-12-09
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

None listed

Interventions

Others(COSMTETICS) : 12 closed patches were applied to 3 areas of the back (non-treated, positive control, test group). 0.3ml of the test product was applied and sealed.

Sponsors

Dr. Raymond Lab Inc
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adults aged 20-40 with a Global Acne Grading System (GAGS) score of 1-30 who voluntarily signed the consent form

Exclusion criteria

Exclusion criteria: Pregnant/breastfeeding women, sensitive skin, presence of skin abnormalities on the test site, or those with recent use of similar products/procedures

Design outcomes

Primary

MeasureTime frame
Follicle/Comedone Ratio

Secondary

MeasureTime frame
Adverse Reaction Assessment

Countries

Korea, Republic of

Contacts

Public ContactMINYEOL CHANG

SKINMED

mychang195@gmail.com+82-42-5118-8437

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Mar 20, 2026