New cream for scalp psoriasis: patients report better satisfaction and quality of life
NCT ID NCT05811234
First seen Jun 24, 2026 · Last updated Jun 26, 2026 · Updated 2 times
Summary
This study followed 291 adults with mild-to-moderate scalp psoriasis who were prescribed a cream containing calcipotriene and betamethasone (Wynzora®). Researchers measured how satisfied patients were with the treatment, its effect on quality of life, and how well it worked in real-world settings over 12 weeks. The goal was to see if the cream improves daily life and symptom control beyond what is seen in controlled clinical trials.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Calcipotriene/Betamethasone dipropionate cream (Wynzora®)
- What this could lead to
- If successful, this could show that the cream improves treatment satisfaction and quality of life for people with scalp psoriasis in everyday use.
- What could go wrong
- This is an observational study, not a controlled trial, so results may be less reliable. It also only looks at short-term outcomes (12 weeks) and may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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291 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Oct 2024
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult male and female participants with mild-to-moderate plaque psoriasis of the scalp will be observed in this study.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adult (greater than or equal to \[\>=\] 18 years) male or female participants with mild-to-moderate plaque psoriasis of the scalp (defined as scalp-PGA score of 2 or 3 at baseline) with or without involvement of the trunk and limbs, and who may or may not have been previously treated (treatment-naive participants) with other anti-psoriatic therapies. 2. Participants who have been prescribed CAL/BDP PAD cream (Wynzora®) treatment to manage plaque psoriasis of the scalp according to SmPC in routine clinical practice. 3. Willingness and ability to participate in the study; participants must give their written consent to participate. Exclusion Criteria: 1. Participants with severe plaque psoriasis, per physician global assessment. 2. Participants with erythrodermic, exfoliative or pustular psoriasis. 3. Participants previously treated with systemic drugs for psoriasis (conventional or biologic) within the last 12 weeks prior to inclusion. 4. Concomitant systemic treatment with anti-psoriatic drugs. 5. Concomitant treatment of any type for plaque psoriasis of the scalp. 6. Hypersensitivity to the active substances or to any of the excipients of CAL/BDP PAD cream (Wynzora®). 7. Participants with known disorders of calcium metabolism. 8. Participants with viral (e.g., herpes or varicella) lesions of the skin, fungal or bacterial skin infections, parasitic infections, skin manifestations in relation to tuberculosis, perioral dermatitis, atrophic skin, striae atrophicae, fragility of skin veins, ichthyosis, acne vulgaris, acne rosacea, rosacea, ulcers, and wounds. 9. Pregnant or breastfeeding women, except when the potential benefit justifies the potential risk. 10. Participants unable to comply with the requirements of the study or who in the opinion of the study physician should not participate in the study. 11. Participants for whom medical chart is inaccessible to physicians to complete baseline data collection.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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DE01
Mannheim, Germany
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DE02
Potsdam, Germany
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DE03
Mönchengladbach, Germany
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DE04
Pforzheim, Germany
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DE05
Mölln, Germany
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DE06
Cologne, Germany
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DE07
Augsburg, Germany
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DE08
Freising, Germany
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DE10
Mainz, Germany
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DE11
Remscheid, Germany
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DE12
Ahaus, Germany
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ES01
Zaragoza, Spain
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ES02
Barcelona, Spain
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ES03
Granollers, Spain
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ES04
Alcorcón, Spain
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ES05
Bilbao, Spain
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ES06
Barcelona, Spain
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ES07
Lleida, Spain
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ES08
Pontevedra, Spain
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ES09
Barcelona, Spain
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ES10
Badalona, Spain
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ES11
Seville, Spain
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ES12
Salamanca, Spain
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ES13
Seville, Spain
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UK01
London, United Kingdom
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UK02
Chertsey, United Kingdom
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UK03
Crewe, United Kingdom
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UK04
Salisbury, United Kingdom
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UK05
Saint Neots, United Kingdom
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UK06
Chipping Norton, United Kingdom
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UK07
Exeter, United Kingdom
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UK08
Cockermouth, United Kingdom
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UK10
Blackburn, United Kingdom
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UK11
Leicester, United Kingdom
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UK12
Wellingborough, United Kingdom
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UK14
Glasgow, United Kingdom
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UK15
Kirkcaldy, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a Once-Daily cream tame psoriasis in toddlers?