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CompletedNCT05770271Updated Apr 25, 2024

The Novel Electrolyzed Water Spray Treatment Mild Senile Groin Eczema, Neurodermatitis and Psoriasis

An interventional study of The novel electrolyzed water spray in Groin Infection, Neurodermatitis and Psoriasis, sponsored by Dove Medical Press Ltd. Completed at 1 site in China. Open to participants aged 35 Years to 55 Years. Per ClinicalTrials.gov, last updated 2024-04-25.

Sponsored by Dove Medical Press Ltd · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
21
Allocation
Not applicable
Ages
35 Years to 55 Years
Sex
All
01

Study summary

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

Read the 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 senile groin eczema, neurodermatitis and psoriasis.

02

Conditions studied

  • Groin Infection
  • Neurodermatitis
  • Psoriasis
  • Eczema

Keywords

  • Electrolyzed water device
  • Hydroxyl radical
  • Tap water
  • Spray
  • Itching
03

In context

Neurodermatitis

34 studies on the registry are indexed under Neurodermatitis; 6 are open to participants now.

This study's enrollment of 21 is below the median of 54 across 32 interventional studies indexed under Neurodermatitis.

Browse Neurodermatitis studies →

Lead sponsor

Dove Medical Press Ltd is the lead sponsor of 11 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • mild senile groin eczema, neurodermatitis and psoriasis.

Exclusion criteria

Exclusion Criteria:

  • severe senile groin eczema, neurodermatitis and psoriasis.
  • people with cognitive disorders.
  • 80 years or older.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
21 participants (actual)

Study arms

  • Experimental
    The mild senile groin eczema, neurodermatitis and psoriasis and one treatment

    Participants with itching of mild senile groin eczema, neurodermatitis and psoriasis will receive one treatment with the device and complete the questionnaire.

    Device: The novel electrolyzed water spray

Interventions

  • DeviceThe novel electrolyzed water spray

    Study staff will use the novel electrolyzed water spray device and spray for approximately 5 minutes on the participant's diseased area until half a bottle (200ml) of water is used. The patients use electrolyzed water to treat the diseased area, two times a day, for 10 days. The trial consists of 10 study visits (day 1-day 10). The relief of mild senile groin eczema, neurodermatitis and psoriasis 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.

06

What researchers measure

Primary outcomes

  1. An itching scale made by modifying the Numeric Pain Rating Scale (NPRS)

    This Score is based on descriptions of the itching that patients rate 0-10 to assess the condition of their itching. A higher score means a worse outcome. 0 means "no itching " and 10 means "the most itching".

    Time frame: 1 hour

Secondary outcomes

  1. A skin signs scale made by modifying the Numeric Pain Rating Scale (NPRS).

    The signs of skin chronic inflammation include darkness or redness, swelling and dryness and broken surface and reduced area of the diseased skin. This Score is based on descriptions of signs of senile groin eczema, neurodermatitis and psoriasis rated 0-10 to assess the condition of mild inflammation of the skin and groin. A higher score means a worse outcome.

    Time frame: 10 days

07

Study locations

1 site
  • Huinuode Biotechnology Co., Ltd.
    Qingdao, China
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Clinical study report

Time frame: until publication of this clinical study and international patent granted

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 25, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05770271
Lead sponsor
Dove Medical Press Ltd
Responsible party
Sponsor
First posted
Mar 15, 2023
Start date
Jan 29, 2023
Primary completion
Jul 20, 2023
Completion
Jan 20, 2024
Last update
Apr 25, 2024

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.

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