Open Label Study Evaluating the Efficacy and Safety of JUVÉDERM VOLUMA™ XC for the Facial Temporal Regions

NACompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

August 7, 2015

Primary Completion Date

April 5, 2017

Study Completion Date

April 5, 2017

Conditions
Aging
Interventions
DEVICE

JUVÉDERM VOLUMA™ XC

Subjects will receive up to 4, 1mL syringes of JUVÉDERM VOLUMA™ XC for their initial injection and a maximum of 6, 1mL syringes of JUVÉDERM VOLUMA™ XC for the study. Subjects will undergo one touch-up injection approximately 2 weeks post initial treatment, and will continue to be evaluated at month 1, month 3, month 6, month 9, and month 12.

Trial Locations (1)

33137

Baumann Cosmetic and Research Institute, Miami

All Listed Sponsors
lead

Baumann Cosmetic and Research Institute

OTHER

NCT02437903 - Open Label Study Evaluating the Efficacy and Safety of JUVÉDERM VOLUMA™ XC for the Facial Temporal Regions | Biotech Hunter | Biotech Hunter