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Clinical Trial Summary

The primary objective of this study is to validate controlled methods of wound, including 1%w/v SLS, 3%w/v SLS, and 24-24 times tape stripping, on the forearms of subjects. The study aims to standardize the procedures for creating wounds and systematically evaluate the effects of these methods on various skin parameters.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06379516
Study type Interventional
Source NovoBliss Research Pvt Ltd
Contact
Status Completed
Phase N/A
Start date January 17, 2024
Completion date February 16, 2024