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Clinical Trial Summary

The purpose of this study is to determine the SPF and UVAPF of four sunscreen formulations using international standard methodologies ISO24444:2010 for SPF and ISO24443:2012 for UVAPF.


Clinical Trial Description

This study consist of two steps. Step 1: determination of the SPF of the test products which will be performed as a single-center, randomized, evaluator blind, intra-individual comparison, no treatment and positive controlled clinical study as per ISO24444:2010. And Step 2: determination of the UVAPF of the test products which will be performed as a single center, open-label, negative and positive controlled technical test as per ISO24443:2012 (using test plates for assessing UV transmittance of four developmental sunscreens). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03157583
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date June 21, 2017
Completion date July 7, 2017

See also
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