Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE2
60 participants
INTERVENTIONAL
2023-03-20
2024-08-31
Brief Summary
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Currently, pharmacological treatments such as retinoids, corticosteroids, vitamin D analogs and biologics remain the main options for most psoriasis patients. However, side effect and high cost barred many ordinary psoriasis patients.
A Chinese medicine formula "Inflammatory skin disease formula (ISDF)" was prescribed by Prof. Lin for many years and observed to be effective in relieving atopic dermatitis and psoriasis patients' clinical manifestations.
In this study, subjects with psoriasis will be randomized into treatment group of "ISDF" or placebo group for 12 weeks.
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Detailed Description
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Recent study demonstrated that ISDF (named SZF in the study) markedly decreased the epidermal thickening and infiltration of mast cells in the ears and dorsal skin of the DNCB-treated mice via inhibition of inflammation through inactivation of NF-κB p65 pathway. The ISDF was found to contain baicalin (4.92%, w/w), berberine (2.90%, w/w), paeoniflorin (0.26%, w/w) and phillyrin (0.10%, w/w). Recent preliminary data revealed that ISDF significantly improved the psoriatic-like symptoms and reduced the epidermal thickening in the dorsal skin of IMQ-stimulated mice via inhibition of the inflammation response. The results on its acute toxicity demonstrated that ISDF at up to the dose of 37.8 g/kg, which was the maximum tolerable dose of ISDF in mice, did not exert any overt toxicity. Based on these positive findings of pilot study, the investigators therefore hypothesize that ISDF is an effective herbal formula with anti-psoriatic effects. In Chinese medicine (CM) theory, psoriasis may be classified into different subtypes or "syndromes", including syndrome of wind-heat and blood heat, which is also known as blood heat syndrome or syndrome of wind-heat and blood dryness; syndrome of blood deficiency and wind-dryness; syndrome of blood stasis in the skin; and dampness-heat syndrome. Each of these syndromes represents a different pathogenesis in CM and corresponds to a different stage or manifestation of psoriasis. ISDF is composed of herbal medicines that can clear heat to cool the blood, clear heat and dry dampness, clear heat and drain dampness, disperse wind-heat, and is suitable for treating psoriasis with wind-heat, blood heat or dampness-heat. A randomized, double-blinded, placebo-controlled trial will be conducted to evaluate the efficacy of ISDF on psoriasis patients. Clinical evidence for the anti-psoriatic effects of ISDF, and is a necessary step towards developing this Chinese medicine formula into an anti-psoriatic pharmaceutical agent.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Inflammatory skin disease formula (ISDF)
Subjects will receive ISDF granules (10.85g twice daily) for 12 weeks.
Inflammatory skin disease formula
ISDF granules (10.85g twice daily) for 12 weeks
Placebo
Subjects will receive placebo granules (10.85g twice daily) for 12 weeks.
Placebo
Placebo granules (10.85g twice daily) for 12 weeks
Interventions
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Inflammatory skin disease formula
ISDF granules (10.85g twice daily) for 12 weeks
Placebo
Placebo granules (10.85g twice daily) for 12 weeks
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Willingness to give informed consent.
Exclusion Criteria
* Psoriatic arthritis with syndrome of spleen-kidney yang deficiency according to Chinese medicine theory.
* Systemic therapy for psoriasis 6 months prior to baseline.
* Use topical medications for psoriasis 14 days prior to baseline such as retinoids, corticosteroids, vitamin D analogues, tazarotene and tacrolimus.
* Has taken any antibiotics, probiotics and prebiotics 30 days prior to baseline.
* UV light therapy 30 days prior to baseline.
* Clinically significant laboratory abnormality in blood, liver or renal functions (≥1.5 times the upper limit of reference range).
* History of allergy to Chinese herbs.
* Unwillingness to comply with study protocol.
* Any other condition that in the opinion of the investigators could compromise the study.
18 Years
75 Years
ALL
No
Sponsors
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Chinese University of Hong Kong
OTHER
Responsible Party
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Prof. Lin Zhixiu
Professor
Principal Investigators
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Zhixiu Lin, PhD
Role: PRINCIPAL_INVESTIGATOR
Hong Kong Institute of Integrative Medicine
Locations
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Hong Kong Institute of Integrative Medicine
Hong Kong, , Hong Kong
Countries
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Central Contacts
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Facility Contacts
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Zhixiu LIN
Role: primary
Other Identifiers
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Psoriasis study
Identifier Type: -
Identifier Source: org_study_id
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