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Clinical Trial Summary

The primary endpoint is the change of the itching score after 3 days of the product use in comparison to the basal value.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05732337
Study type Interventional
Source Karo Pharma AB
Contact
Status Completed
Phase N/A
Start date January 30, 2023
Completion date July 5, 2023

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