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Clinical Trial Summary

The study will be a prospective, randomized, split-face, double blind, controlled, clinical trial to evaluate the safety and effectiveness of Lumina™ for the treatment of Nasolabial Folds (NLFs). Subjects will be randomized to receive treatment (Lumina™) in one NLF and control (Restylane® Defyne) in the contra-lateral NLF. 118 subjects will be treated.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04839484
Study type Interventional
Source LifeSprout, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date March 2, 2021
Completion date March 2023

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