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Intact Skin clinical trials

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NCT ID: NCT04192123 Completed - Intact Skin Clinical Trials

Open-Label Test of the HM242 Medical Devices to Evaluate Safety and Local Tolerability

Start date: May 25, 2020
Phase: N/A
Study type: Interventional

It is the first clinical study aimed at assessing the safety and tolerability of HM242-Solution and HM242-Gel after their application under occlusion on intact skin. The HM242-Solution is intended for chronic wounds (e.g. pressure, venous leg and diabetic foot ulcers). The HM242-Solution should be used for physical rinsing and cleansing and subsequent decolonization of the wound prior to treatment with hydrogels and dressings. The HM242-Gel is a hydrogel for wound bed preparation to support the healing of the skin due to cleansing, moistening and subsequent decolonization and the coating of the wound. The study will be conducted in outpatient manner, adult patients who are healthy and has an intact skin. This is an prospective, open label, monocentric study. No comparative control group is planned as no other preventing infection solution is commercially available at this time.

NCT ID: NCT03007264 Completed - Intact Skin Clinical Trials

Cold Plasma for Wound Treatment, Safety Study

Start date: June 18, 2018
Phase: Phase 1
Study type: Interventional

In this study the application of cold atmospheric plasma (CAP) will be tested on intact skin of volunteers. To test safety, several skin parameters will be monitored, the antimicrobial effect will be investigated as well. The investigators expect this treatment to have a good antimicrobial effect with acceptable, transient skin sensations.