Novel Electrolyzed Water Spray Treatment Mild Dermatophytosis
- Conditions
- Dermatophytoses
- Interventions
- Device: The novel electrolyzed water spray
- Registration Number
- NCT05770245
- Lead Sponsor
- Dove Medical Press Ltd
- Brief Summary
The purpose of this study is to test whether spraying the skin of patients of patients by use of the novel electrolyzed water spray will produce improvement in the condition of mild dermatophytosis.
- Detailed Description
In this study, water inculding tap water,pure water and salt water, and an apparatus for producing electrolyzed water (https://www.deposon.com.cn; https://www.deposon.com）were used to generate an electrolyzed water mist spray or spray. This instantly generated electrolyzed water mist spray or spray has oxidation-reduction potential (ORP) ≥1200mv,and contains non-specific total oxidation capacity which equals to 0.28±0.10ppm,0.06±0.04ppm and 3.92±0.39ppm of desolved ozone. This instantly generated electrolyzed water mist spray or spray does not release detectable ≥0.1mg/m3 of gaseous ozone. This instantly generated electrolyzed water mist spray or spray has pH 8.4±0.4 and releases negative air ion.The apparatus for producing electrolyzed water has a positive electrode which is covered by a conductive diamond material (Patent# CN215308550U).This is an open-label, single-arm, and before and after treatment comparison study. This study uses this novel electrolyzed water device and the water spray to treat mild dermatophytosis.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 14
- mild dermatophytosis accompanied by significant itching symptom
- Patient > 18 years old.
- severe dermatophytosis.
- 80 years or older.
- Pregnant or breastfeeding women.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Mild dermatophytosis and one treatment The novel electrolyzed water spray Study staff will use the novel electrolyzed water spray device and spray for approximately 10 minutes on the participant's diseased area until half a bottle (200ml) of water is used.
- Primary Outcome Measures
Name Time Method An itching scale made by modifying the Numeric Pain Rating Scale (NPRS) 7 days This Score is based on descriptions of the itching that patients rate 0-10 to assess the condition of their mild dermatophytosis. A higher score means a worse outcome. 0 means "no itching " and 10 means "the most itching".
- Secondary Outcome Measures
Name Time Method A skin signs scale made by modifying the Numeric Pain Rating Scale (NPRS). 7 days The skin signs scale evaluates the disease-damaged skin replaced by fresh and healthy skin. This Score is based on descriptions of darkness or redness, swelling and dryness, broken surface, and reduced diseased skin area patients rate 0-10. A higher score means a worse outcome.
Trial Locations
- Locations (1)
Huinuode Biotechnology Co., Ltd.
🇨🇳Qingdao, China