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Clinical Trial Summary

The study will be performed with oral gels, with up to 55 study subjects who meet the inclusion and non-inclusion criteria required. Study subjects will be instructed to use the products during 12 weeks and they will be assessed and supervised throughout the study by clinic technicians, in order to check for possible adverse events. Efficacy documentation through digital photography, instrumental measurements with the devices Cutometer® MPA 580 and Tewameter®, image acquisition with Visia-CA® as well as self-assessment through questionnaires will be carried out.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05328388
Study type Interventional
Source LycoRed Ltd.
Contact
Status Completed
Phase N/A
Start date January 1, 2022
Completion date March 15, 2022

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