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CLINICAL EVALUATION OF THE EFFICACY OF A HY-CBD ANTI-ACNE GEL IN REDUCING THE NUMBER OF ACNE AND REDUCING THE SEVERITY OF INFLAMMATORY ACNE

CLINICAL EVALUATION OF THE EFFICACY OF A HY-CBD ANTI-ACNE GEL IN REDUCING THE NUMBER OF ACNE AND REDUCING THE SEVERITY OF INFLAMMATORY ACNE

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250507005
Enrollment
20
Registered
2025-05-07
Start date
2023-02-06
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Inflammatory acne Skin Diseases Acne Vulgaris

Interventions

Hy-CBD Anti-Acne Gel, formulated with 3% w/w CBD-loaded HA-pNIPAM nanogel, was developed by the Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand. This product is designe
Hy-CBD Anti-Acne Gel

Sponsors

NABSOLUTE CO., LTD
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Subject having inflammatory acnes on face.

Exclusion criteria

Exclusion criteria: For women: pregnant or nursing woman or woman planning to get pregnant during the study Cutaneous pathology on the study zone (eczema, etc) Subject has history of allergy to cosmetic products Retinoids during the six previous months of the study Acne treatment (except retinoids) since less than one month Any change in hormonal treatment (including contraceptive) during the three previous months of the study Use of topical or systemic treatment during the previous weeks liable to interfere with the assessment of the cutaneous acceptability/efficacy of the study product Subject went through dermatologist treatments or procedures within 2-month period before the study start Subject having undergone a surgery under general anesthesia within the previous month Excessive exposure to sunlight or UV-rays within the previous month Subject enrolled in another clinical trial during the study period Subject considered by the investigator to be likely not compliant to the protocol.

Design outcomes

Primary

MeasureTime frame
Reduce condition of inflammatory acne After 2 and 7 days of use the product Clinical scoring and measurement size using a vernier calliper by the dermatologist

Secondary

MeasureTime frame
Cutaneous acceptability After 2 and 7 days of use the product Clinical signs observed Functional and physical signs reported

Countries

Thailand

Contacts

Public ContactSujittra Sombuntham

Dermscan Asia

technical@dermscanasia.com029374377

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026