NCT06800755Completed
Evaluation of the Efficacy and Tolerance of the Medical Device RL3020-DP0364 in Adult Population With Stable Mild Plaque Psoriasis, Dry Skin and Pruritus
Source: ClinicalTrials.gov · Last updated 5 May 2026
Brief summary (registry, in English)
The product RL3020-DP0364 developed by Pierre Fabre Laboratories moisturizes durably and repairs dry or atopic skin, especially in the case of certain dermatoses (atopic dermatitis, ichthyosis, etc ...) and erythema induced by radiotherapy. Its unique formula treats the symptoms of dry skin by creating a protective film that prevents dehydration and helps protect the skin from external aggressions. Through this study, the efficacy of this medical device will be evaluated specifically in subjects presenting stable psoriasis, dry skin and pruritus with an application on the whole body (excluding the head).
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 40 (actual)
- First submitted
- 24 Jan 2025
- Start date
- 27 Feb 2025
- Primary completion date
- 10 Jul 2025
- Lead sponsor
- Pierre Fabre Dermo Cosmetique
- Diseases
- Psoriasis
- NCT number
- NCT06800755
What you commit to
- Study type: Interventional
- Participants enrolled: 40
- From 27 Feb 2025 to the primary completion date, 10 Jul 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Biotherapy treatment in the 6 months prior to the inclusion visit or ongoing or planned to be started during the study
- Other systemic treatment for psoriasis (acitretin, cyclosporine, methotrexate, apremilast...) in the 3 months prior to the inclusion visit or ongoing or planned to be started during the study
- Phototherapy treatment in the 4 weeks prior to the inclusion visit or ongoing or planned to be started during the study
- Any other systemic treatment incompatible with the study or liable to interfere with the study assessments according to the investigator, in the weeks prior to the inclusion visit, ongoing or planned to be started during the study
- Topical treatment for psoriasis (corticosteroid, vitamin D analogs…) applied on the body\* in the 4 weeks prior to the inclusion visit or ongoing or planned to be started during the study
- Topical product (including any moisturizer, emollient, keratolytic …) applied on the body\* in the 7 days prior to the inclusion visit or ongoing or planned to be started during the study
- Any other topical treatment or product applied on the body\* incompatible with the study or liable to interfere with the study assessments according to the investigator, in the weeks prior to the inclusion visit, ongoing or planned to be started during the study
- the head is not included in the evaluated area
Other illness
- Criteria related to the disease:
- Subject with history of allergy or intolerance to any of the tested product ingredients
- Subject having any other dermatologic condition than psoriasis, or characteristics (like tattoo, wound…) on body liable to interfere with the study assessments
- Subject having an acute, chronic or progressive disease or history of disease liable to interfere with the study data or considered by the Investigator hazardous for the subject or incompatible with the study requirements
- Criteria related to treatments and/or products:
Other
- Subject with erythrodermic psoriasis, pustular psoriasis
- Subject with palmoplantar keratoderma
- Subject with any other aetiology of pruritus, not related to plaque psoriasis
- Any product applied on the body\* before the visit, the day of inclusion visit
Who the study is looking for
- Subject with stable mild plaque psoriasis covering ≤ 10% BSA (Body Surface Area; excluding the head\*)
- Subject whose plaque psoriasis has been diagnosed for at least 6 months before the inclusion visit
- Subject with dry skin according to the investigator assessment
- Subject with a pruritus intensity (on average over the previous 24 hours) ≥ 3 on a Numerical Rating Scale (NRS) between 0 and 10 (with 0 = no pruritus and 10 = worst imaginable pruritus) on the body\*
- the head is not included in the evaluated area
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Dermscan Poland Coordinator of this site? Confirm its status | Gdansk | Poland | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.