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NOT YET RECRUITING
NCT07501442
NA

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

Sponsor: Wooshin Labottach Co., Ltd.

View on ClinicalTrials.gov

Summary

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

Official title: A Randomized, Single Blind, Parallel Groups, Clinical Trial Evaluating the Efficacy and Safety of Uracil 0,5%-Containing Plasters Versus "Lenitive Cream", in Oncology Patients Affected by Hand-foot Syndrome (HFS)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2026-07

Completion Date

2027-04

Last Updated

2026-03-30

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Uracil 0,5% plasters

Patients will applicate to hands and feet the plaster twice per day for 3 weeks to reduce the HFS grade.

DEVICE

lenitive cream

Patients will applicate the cream 3 times per day for 3 weeks to compare the change of HFS severity

Locations (1)

Presidio Ospedaliero Di Rho - Asst Rhodense- Oncology Department

Rho, MI, Italy