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SAFETY AND EFFECTIVENESS OF OXYRESVERATROL CREAM IN HEALTHY VOLUNTEERS AND PATIENT WITH DERMATITIS

SAFETY AND EFFECTIVENESS OF OXYRESVERATROL CREAM IN HEALTHY VOLUNTEERS AND PATIENT WITH DERMATITIS

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240611001
Enrollment
40
Registered
2024-06-11
Start date
2024-07-01
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

patients with dermatitis Oxyresveratrol, Dermatitis, Eczema

Interventions

The cream formulation combines 0.1% Oxyresveratrol,Cetyl alcohol, PEG-40 Stearate, 1,3Butylene Glycol, Biosaccharide Gum, Phenoxyethanol, Water,The cream formulation combines 0.5% Oxyresveratrol,Cet
Active Comparator Other,Active Comparator Other,Active Comparator Other,Placebo Comparator Other
oxyresveratrol cream A,oxyresveratrol cream B,oxyresveratrol cream C,oxyresveratrol cream D

Sponsors

Ratchadapisek Research Fund - Type 2
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis with acute to subacute eczema by dermatologist at OPD King Chulalongkorn Memorial hospital 2. At least 1 lesion of acute to subacute eczema with mild severity with 0-12 Eczema Area and Severity Index score

Exclusion criteria

Exclusion criteria: 1. wide-spread systemic skin diseases 2. other skin lesion at the area of study 3. history of ORV allergy 4. pregnant or lactation 5. received topical immunosuppressant or corticosteroid within 2 weeks 6. received oral immunosuppressant or corticosteroid within 4 weeks 7. received live vaccine or immunotherapy within 4 weeks 8. patients with cancer or autoimmune disease

Design outcomes

Primary

MeasureTime frame
Eczema Area and Severity Index (EASI) baseline, 3 days, 7 days, 14 days, and 28 days (range from 0 to 72)

Secondary

MeasureTime frame
Biophysical changes of skin (skin hydration, trans-epidermal water loss, pH) baseline, 3 days, 7 days, 14 days, and 28 days using Corneometer (unit from 0 (no water at all) - 120 (on water)), Tewameter (g/m2/h), and pH meter(a scale of 0 to 14)

Countries

Thailand

Contacts

Public ContactJongkonnee Wongpiyabovorn

Faculty of Medicine, Chulalongkorn University

jongkonneew@gmail.com662564455

Outcome results

None listed

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