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Clinical Trial Summary

This will be a single-center, randomized, evaluator-blinded, split-face clinical study design. Fifty patients will receive one treatment session consisting of Restylane® Silk (right side of the face) and Belotero Balance® (left side), or vice versa (1:1 dose conversion ratio) injections to the superficial, vertical perioral lines. Injections will be performed at the baseline visit. To ensure subject and investigator blinding, syringes will be prepared and labeled "1" and "2" immediately before subject attendance for injection by the sub-investigator. The same injection sites and techniques will be used on both sides of the face. Then, patients will follow-up on post-treatment day 7, 14, 30, 60, 90, 120, 150, 180.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02818556
Study type Interventional
Source The Maas Clinic
Contact Rachel Bass
Phone (415)567-8275
Email research@maasclinic.com
Status Recruiting
Phase Phase 4
Start date June 2016

See also
  Status Clinical Trial Phase
Completed NCT03923634 - Princess® RICH for the Correction of Fine Lines N/A
Completed NCT03092219 - RHA Redensity - Perioral Rhytids N/A