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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05766930
Other study ID # jia19951210
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 29, 2023
Est. completion date March 1, 2024

Study information

Verified date February 2023
Source Dove Medical Press Ltd
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to test whether spraying the genitalia of patients by use of the novel electrolyzed water spray will produce improvement in the condition of genitalia itching.


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 genital itching.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date March 1, 2024
Est. primary completion date July 15, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 62 Years
Eligibility Inclusion Criteria: Patients with genital itching. Exclusion Criteria: Severe genital itching. 80 years or older.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
The novel electrolyzed water spray
Study staff will use the novel electrolyzed water spray device and spray for approximately 2-4 minutes on the participant's diseased area until half a bottle (20-40ml) of water is used. The patients use electrolyzed water to treat the diseased area, two times a day, for 5 days. The trial consists of 5 study visits (day 1-day 5). The relief genital itching evaluation and adverse event assessments will be performed at each visit. Safety analysis will be assessed based on the reports of adverse events during the study.

Locations

Country Name City State
China Huinuode Biotechnology Co., Ltd. QingDao

Sponsors (1)

Lead Sponsor Collaborator
Dove Medical Press Ltd

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary An itching scale made by modifying a pain scale (NPRS) This Score is based on descriptions of the itching that patients rate 0-10 to assess the condition of their genitalia with itching. A higher score means a worse outcome. 0 means "no itching " and 10 means "the most itching". 5 days
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