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Clinical Trial Summary

This study is to determine the efficacy and safety of JUVÉDERM VOLUMA™ XC when used in the facial temporal regions based on the change in the score of the investigator's Temporal. This study will be an open label, single center study.


Clinical Trial Description

Volume deficit in the temporal area (the side of the forehead) of the face is a common sign of aging.

JUVÉDERM VOLUMA™ XC is a dermal filler, which was FDA-approved in October 2013 for the improvement and correction of age-related volume deficit in the mid-face area.

JUVÉDERM VOLUMA™ XC is a gel implant composed of 20 mg/mL hyaluronic acid (HA) formulation, produced by Streptococcus equi bacteria, and 0.3 w/w lidocaine. JUVÉDERM VOLUMA™ XC is a clear, sterile, and biodegradable gel indicated for subcutaneous and/or supraperiosteal injection.

JUVÉDERM VOLUMA™ XCwill be injected in the temple area and subjects will be followed for 12 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02437903
Study type Interventional
Source Baumann Cosmetic and Research Institute
Contact
Status Completed
Phase N/A
Start date August 7, 2015
Completion date April 5, 2017

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