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Multi-center, Phase Ⅳ, Single Arm, Open-label Clinical Trial to Evaluate the Efficacy and Safety of Meditoxin® in Subjects With Essential Blepharospasm
The purpose of this study is to evaluate the efficacy and safety of Meditoxin® in the treatment of Essential blepharospasm.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Sevrance Hospital
Seoul, South Korea
Seoul St.Mary Hospital
Seoul, South Korea
Chung-Ang Univesity Yongsan Hospital
Seoul, South Korea
Start Date
August 1, 2010
Primary Completion Date
May 1, 2011
Completion Date
August 1, 2011
Last Updated
April 25, 2012
110
ACTUAL participants
Botulinum Toxin Type A
DRUG
Lead Sponsor
Medy-Tox
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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