A Multi-center Acute Efficacy Trial of GFX For Reduction of Glabellar Furrowing

Forehead Wrinkles Clinical Trial

Official title: A Multi-center Acute Efficacy Trial of GFX For Reduction of Glabellar Furrowing

Status Completed

Clinical Trial Summary

The purpose of this research study is to evaluate the immediate effectiveness of the GFX™ device in reducing the furrows (deep frown lines) between eyebrows (glabellar region).

Clinical Trial Description

The purpose of this research study is to evaluate the acute ability of GFX to reduce glabellar furrowing.

Patients who have presented to the investigator for correction of glabellar furrows, as classified per the Rated Numeric Kinetic Line Scale Score for Facial Wrinkles Secondary to Hyperkinetic Function (Note: Class 1 or Higher)7 (Appendix N) are candidates for this study. All patients must consent to the procedure and agree to complete their post treatment evaluation visit. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Forehead Wrinkles
• Glabellar Furrowing

• NCT number: NCT00612378
• Study type: Interventional
• Source: Advanced Cosmetic Intervention
• Status: Completed
• Phase: N/A
• Start date: September 2007
• Completion date: March 2008