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Efficacy assessment of PURICAS DRAGON'S BLOOD SCAR GEL on acne spot reduction

Efficacy assessment of PURICAS DRAGON'S BLOOD SCAR GEL on acne spot reduction

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220222001
Enrollment
33
Registered
2022-02-22
Start date
2021-02-25
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Healthy male or female Thai volunteers aged between 20-50 years old acne spot reduction

Interventions

Spectrophotometer, Corneometer and Visia CR are used to assess skin condition and color of red or dark spots before using the product and after using the product for 1,3,7 and 14 days
Experimental Other
PURICA&#039
S BLOOD SCAR GEL

Sponsors

NATURA REMADEE COMPANY LIMITED
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Healthy male or female aged between 20-50 years old 2. Having at least 2 visible red or/and dark spots from acne on the face (diameter not less than 5 mm) 3. Be able to read, write and communicate Thai language 4. Having consent in the study after being informed objective, methodology, possible risk and result, and be able to follow the study protocol

Exclusion criteria

Exclusion criteria: 1. Pregnancy or lactation 2. Having allergic history to counter brand cosmetic products 3. Having history of eczema or psoriasis within 6 months before enrollment in the study 4. Having history of steroid, antibiotic, non-steroidal anti-inflammatory or antihistamine drug use within 3 days before enrollment in the study 5. Using any products related to anti-acne in 14 days before participating in the study 6. Regular smoking or drinking 7. Having history of participating about anti-acne clinical research project running within 3 months before enrollment in the study

Design outcomes

Primary

MeasureTime frame
Skin erythema and brightening 14 days Measuring by Spectrophotometer,Moisture content 14 days Measuring by Corneometer,Facial skin measurement in 3D 14 days The photographed of facial area by VISIA CR

Secondary

MeasureTime frame
N/A N/A N/A

Countries

Thailand

Contacts

Public ContactNeti Waranuch

Naresuan university, Phitsanulok, Thailand

cosnat@nu.ac.th055968801

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026