Facial Wrinkles and Rhytides Reduction Clinical Trial
Official title:
Clinical Study to Determine Safety and Efficacy of FPlus for Wrinkle Treatment
Patient demand for non-surgical, non-invasive, and no-downtime wrinkle and rhytides
treatment procedures has grown dramatically over the past decade as new treatments and
technologies have been introduced.
This study was performed in order to evaluate the efficacy and safety of the Invasix FPlus
System, an innovative noninvasive system intended for wrinkles and rhytides treatment.
Subjects were treated for face wrinkles and rhytides reduction and followed for 3 months
after last treatment. In order to evaluate treatment efficacy, pre and post treatment photos
were introduced to three uninvolved physicians for blinded evaluation.
n/a
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment