Actively Recruiting
Study to Assess Efficacy, Safety and Tolerability of a Nail Patch in Patients With Nail Fragility, Mychosis, Psoriasis
Led by Wooshin Labottach Co., Ltd. · Updated on 2026-01-26
72
Participants Needed
1
Research Sites
43 weeks
Total Duration
On this page
Sponsors
W
Wooshin Labottach Co., Ltd.
Lead Sponsor
N
Nextrasearch S.r.l.s.
Collaborating Sponsor
AI-Summary
What this Trial Is About
A randomized, double blind, placebo-controlled, unicenter, parallel group study to assess the efficacy, safety and tolerability of a multi-funtion toe nail patch in patients affected by nail fragility, nail mychosis and psoriasis 72 patients in 6 subgroups Treatment duration 3 months + 1 month follow-up
CONDITIONS
Official Title
Study to Assess Efficacy, Safety and Tolerability of a Nail Patch in Patients With Nail Fragility, Mychosis, Psoriasis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 years or older
- Nail fragility, distal subungual onychomycosis, or nail psoriasis affecting 75% or less of the nail bed confirmed by photographic documentation and investigator evaluation
You will not qualify if you...
- Proximal subungual onychomycosis extending into the proximal nail or affecting more than 75% of the nail
- Conditions causing abnormal nail appearance, immunosuppression, or severe peripheral circulatory insufficiency
- Use of topical antifungal or anti-psoriasis nail treatments within one month
- Use of systemic antifungal treatments within three months
- Participation in another clinical nail study within the previous three months
- Known allergy to any of the study treatments
- Presence of unrelated nail disorders such as onychomycosis, nail psoriasis, or genetically induced onychodystrophy
- Other nail disorders, active or severe psoriasis elsewhere, or other autoimmune or inflammatory diseases
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Clinica Dermatologica - Policlinico - Università degli Studi di Milano Via Francesco Sforza- Milano
Milan, Italy, 20122
Actively Recruiting
Research Team
A
Adolfo Gasparetto
CONTACT
A
Andrea Borgatta
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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