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Efficacy and Safety of Cream containing Dipotassium Glycyrrhizinate, Vaccinium Myrtillius, Epigallocatechin Gallatyl Glucoside, Tamarindus Indica Compared with Triamcinolone acetonide Cream in the treatment of eczema and plaque psoriasis

Efficacy and Safety of Cream containing Dipotassium Glycyrrhizinate, Vaccinium Myrtillius, Epigallocatechin Gallatyl Glucoside, Tamarindus Indica Compared with Triamcinolone acetonide Cream in the treatment of eczema and plaque psoriasis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20211025002
Enrollment
75
Registered
2021-10-25
Start date
2019-03-04
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

Efficacy and Safety of Cream containing Dipotassium Glycyrrhizinate, Vaccinium Myrtillius, Epigallocatechin Gallatyl Glucoside, Tamarindus Indica Compared with Triamcinolone acetonide Cream in the treatment of eczema and plaque psoriasis Eczema, Plaque type psoriasis, 0.1% Triamcinolone acetonide , Dipotassium glycyrrhizinate acid, Vaccinium Myrtillius, Epigallocatechin Gallatyl Glucoside, Tamarindus Indica

Interventions

Cream containing Dipotassium Glycyrrhizinate, Vaccinium Myrtillius, Epigallocatechin Gallatyl Glucoside, Tamarindus Indica twice daily for 1 month,TA cream twice daily for 1 month
Active Comparator Drug,Active Comparator Drug
Cream containing Dipotassium Glycyrrhizinate, Vaccinium Myrtillius, Epigallocatechin Gallatyl Glucoside, Tamarindus Indica,TA cream

Sponsors

Srinakharinwirot University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. The participants had both sided of eczema or plaque psoriasis with approximately similar severity 2. Older than 18 years

Exclusion criteria

Exclusion criteria: 1. Topical steroid used in the recent 2 weeks 2. Systemic immunosuppressive drugs used in the recent 4 weeks 3. Pregnancy/lactation 4. History of allergic reaction following study cream

Design outcomes

Primary

MeasureTime frame
efficacy and safety 1 month pEASI and pPASI

Secondary

MeasureTime frame
improve of skin barrier function 1 month Transepidermal water loss/skin hydration/DLQI/ clinician assessment

Countries

Thailand

Contacts

Public ContactSiriwan Palawisuth

Punyananthaphikkhu Chonprathan Medical Center

siriwan_monk@yahoo.com025022345

Outcome results

None listed

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