Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Study to Evaluate the Safety and Clinical Performance of a Dexpanthenol Medicated Hydrogel Patch in the Treatment of Standardized Superficial Abrasions

Clinical evaluation of a Dexpanthenol-medicated wound plaster on standardized superficial skin abrasions

Participants needed: 40
Trial details
Age: 18-64Biological sex: AllType: InterventionalSponsor: Wooshin Labottach Co., Ltd.Updated: Jun 16, 2026Locations: 1
Eligibility criteria

Healthy male or female volunteers aged 18 to 64 years (inclusive). [+4]

Known hypersensitivity or allergy to Dexpanthenol, hydrogel components, acrylic... [+8]

Status: Not yet recruiting

Clinical Trial Evaluating the Efficacy and Safety of Uracil 0,5% Plasters in Oncology Patients Affected by Hand-foot Syndrome (HFS)

The goal of this clinical trial is to learn if The Uracil plaster works to treat mild HFS in adults under chemiotherapy. It will also learn about the safety . The main questions it aims to answer are: Does Uracil Plaster lower the number of days participants need to reduce the HFS symptoms? What medical problems do participants have when using the Uracil plaster MD? Researchers will compare the Uracil plaster to a standard lenitive cream to see if Uracil Plaster works better to treat mild HFS. Participants will: Use the plaster or the cream 2/3 times day for 3 weeks Visit the hospital once every week for checkups and tests Keep a diary of their symptoms and the number of times they use the therapy

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Wooshin Labottach Co., Ltd.Updated: Mar 30, 2026Locations: 1
Eligibility criteria

Both sexes; [+6]

Patients with grade III severity according to of HFS severity (Hand-Foot Syndrom... [+10]

Status: Recruiting

Study to Assess Efficacy, Safety and Tolerability of a Nail Patch in Patients With Nail Fragility, Mychosis, Psoriasis

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

Participants needed: 72
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Wooshin Labottach Co., Ltd.Updated: Jan 26, 2026Locations: 1
Eligibility criteria

aged 18 years or older Fragility Nails Distal Subungual Onychomycosis Nail Psori...

Patients that have proximal subungual onychomycosis, if their distal subungual o... [+6]