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To assess the effectiveness of topical tapinarof to topical betamethasone in patients with mild to moderate plaque psoriasis presenting to tertiary care hospital in Islamabad
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Tapinarof 1% cream | Experimental | Participants will apply topical tapinarof 1% cream once daily to effected plaque psoriasis |
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| Betamethasone dipropionate 0.05% | Active Comparator | Participants will apply topical betamethasone dipropionate 0.05% cream/ointment twice daily to effected plaque psoriasis lesions |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Betamethasone Dipropionate 0.05% Cream | Drug | Topical betamethasone dipropionate 0.05% cream once daily applied to affected plaque psoriasis lesions twice daily for up to 4 weeks |
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| Measure | Description | Time Frame |
|---|---|---|
| Percentage of participants achieving a 75% reduction from baseline in psoriasis area and severity index(PASI 75) | The psoriasis area and severity index(PASI) quantifies the severity of psoriasis plaques and the total body surface area affected.It combines assessments of plaque erythema, induration and desquamation across four body regions (head, trunk, upper limbs, lower limbs ) into a score ranging from 0 ( no disease) to 72 ( severe disease) .PASI 75 represents a 75% or greater reduction ( improvement) in the total PASI score compared to the participants baseline value. | 12 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Noor Ul Ain, PGT Dermatology | Contact | +923365788143 | nooraftab146@gmail.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pakistan institute of medical sciences(PIMS) | Islamabad | Federal | 44000 | Pakistan |
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| ID | Term |
|---|---|
| D011565 | Psoriasis |
| ID | Term |
|---|---|
| D017444 | Skin Diseases, Papulosquamous |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
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| ID | Term |
|---|---|
| C011175 | betamethasone-17,21-dipropionate |
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This is a quasi-experimental research(with a single pre-test/post-test group).A quasi-experimental design is acceptable since all eligible patients will get the active intervention (tapinarof) without a placebo control group,which is typical in real world clinical practice.The primary outcome (PASI score) will be assessed at baseline and three follow-up points (weeks 4,8 and 12), allowing for within-subject comparison.
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| Tapinarof Cream 1% | Drug | Topical tapinarof 1% cream applied once daily to affected skin areas for up to 12 weeks |
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