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Evaluation of moisturizing, post-acne blemishes efficacy and satisfaction assessment of sheet mask product containing pectin of Cissampelos pareira L.

Evaluation of moisturizing, post-acne blemishes efficacy and satisfaction assessment of sheet mask product containing pectin of Cissampelos pareira L.

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260226005
Enrollment
30
Registered
2026-02-26
Start date
2026-02-09
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

Post-acne blemishes and skin dehydration in healthy adults Skin Hyperpigmentation Skin Hydration Pectin Cosmetics Volunteers, Healthy

Interventions

Participants will receive an experimental sheet mask containing pectin extracted from Cissampelos pareira L. The mask will be applied to the facial skin for approximately 15 to 20 minutes once daily b
Experimental Other
BOTANISIA BLEMISH SHEET MASK

Sponsors

Mae Fah Luang Intellectual Property Management and Innovation Division (MFii)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Male or female aged 20-40 years 2. Have good health 3. No history of sensitive skin or chronic inflammatory skin diseases (e.g., psoriasis) 4. Have a history of acne with residual hyperpigmentation (dark spots) in previously affected areas, but no active inflammatory acne in the testing area

Exclusion criteria

Exclusion criteria: 1. Pregnant or breastfeeding women 2. Use of products other than the test product under investigation, including immunostimulants, antibiotics, glucocorticosteroids, products containing retinoids or azelaic acid, acne medications, treatments for seborrheic dermatitis, oral contraceptives or any hormonal supplements taken for skin aesthetic purposes. 3. Known allergy to the substances used in the research, specifically pectin extract from Cissampelos pareira L. 4. Participation in other clinical research studies during the same period

Design outcomes

Primary

MeasureTime frame
Skin hydration level Baseline and after 7 consecutive days of product use Corneometer,Melanin index and erythema index Baseline and after 7 consecutive days of product use Mexameter

Secondary

MeasureTime frame
Transepidermal Water Loss Baseline and after 7 consecutive days of product use Tewameter,Skin texture and spot analysis Baseline and after 7 consecutive days of product use Visia skin analysis

Countries

Thailand

Contacts

Public ContactTawanun Sripisut

Mae Fah Luang University

tawanun.sri@mfu.ac.th053916833

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026