ClinicalTrials.Veeva

Menu

Safety and Effectiveness of BOTOX® for Lateral Canthal Lines With or Without Simultaneous Glabellar Lines in Korea

Allergan logo

Allergan

Status

Completed

Conditions

Lateral Canthal Lines
Crow's Feet Lines

Treatments

Biological: Botulinum Toxin Type A

Study type

Observational

Funder types

Industry

Identifiers

NCT02248844
191622-147

Details and patient eligibility

About

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.

Enrollment

667 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject and Investigator decision to treat crow's feet lines with Botox®

Exclusion criteria

  • None

Trial design

667 participants in 1 patient group

Botulinum Toxin Type A
Description:
Subjects who receive botulinum toxin Type A injected into crow's feet line areas per clinical practice.
Treatment:
Biological: Botulinum Toxin Type A

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems