A Study to Evaluate the Effectiveness of Juvéderm® VOLIFT®™ With Lidocaine for Dynamic Radial Cheek Line Skin Depressions

Study Identifier
GMA-EAME-FAS-0397
CT.gov Identifier
NCT02980783
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Study Details

Medical Condition
  • Facial Aesthetics - Fillers
    • Study Drug
    N/A
    Phase
    Phase 4
    Sex
    Female
    Age
    40 - 65 Years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Presence of dynamic radial cheek lines * Agrees not to make any changes to skin care routines, or to have any facial procedures or treatments during the study
    Exclusion Criteria:
    * Previous facial surgery, tissue grafting, or tissue augmentation with silicone, fat, or other permanent, or semi-permanent dermal fillers or be planning to undergo any of these procedures during the study * Undergone temporary facial dermal filler injections with any substance in the face in the 12 months prior to study entry * Received botulinum toxin therapy of any serotype in any facial area within the previous 6 months agrees not to receive it during the study

    Protocol Summary

    This study will evaluate the effectiveness of Juvéderm® VOLIFT®™ with Lidocaine for dynamic radial cheek line skin depressions.

    Study Locations

    Location
    Status
    Location
    Laboratoire DERMSCAN
    Lyon, France, 69100
    Status
    Not applicable