This is a postmarketing surveillance study in Korea to evaluate the safety and effectiveness of BOTOX® for lateral canthal lines (crow's feet lines) with or without simultaneous glabellar lines.
Study Type
OBSERVATIONAL
Enrollment
667
Botulinum toxin Type A injected into crow's feet line areas per clinical practice.
Dr. Robbin Clinic
Gangnam-gu, Seoul, South Korea
Number of Participants with Adverse Events
Time frame: Up to 3 months
Investigator's Assessment of Change in Appearance of Crow's Feet Lines on a 3-Point Scale
Time frame: Baseline, Up to 3 months
Subject's Assessment of Change in Appearance of Crow's Feet Lines on a 7-Point Scale
Time frame: Baseline, Up to 3 months
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