Ignite Creation Date:
2024-05-06 @ 6:43 PM
Last Modification Date:
2024-10-26 @ 2:53 PM
Study NCT ID:
NCT05765526
Status:
COMPLETED
Last Update Posted:
2024-04-25
First Post:
2023-02-27
Brief Title:
A Novel Electrolyzed Water Spray Treatment for the Discomfort or Itching of Patients With Scalp
Sponsor:
Dove Medical Press Ltd
Organization:
Dove Medical Press Ltd
Study Overview
Official Title:
A Novel Electrolyzed Water Spray Reduces Discomfort or Itching Scores of Patients With Scalp Discomfort or Itching A Clinical Study
Status:
COMPLETED
Status Verified Date:
2023-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to test whether the reduction of the discomfort or itching with the scalp of patients by use of the novel electrolyzed water spray will produce improvement in the condition of the scalp
Detailed Description:
In this study water inculding tap waterpure water and salt water and an apparatus for producing electrolyzed water httpswwwdeposoncomcn httpswwwdeposoncomwere used to generate an electrolyzed water mist spray or spray This instantly generated electrolyzed water mist spray or spray has oxidation-reduction potential ORP 1200mvand contains non-specific total oxidation capacity which equals to 028010ppm006004ppm and 392039ppm of desolved ozone This instantly generated electrolyzed water mist spray or spray does not release detectable 01mgm3 of gaseous ozone This instantly generated electrolyzed water mist spray or spray has pH 8404 and releases negative air ionThe 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 In this study this novel electrolyzed water device and the water spray are used to treat scalp itching The reduction in the scalp of discomfort or 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None