drugset / Trial / NCT00276315

Assessment of Effectiveness and Safety of Dysport® for the Treatment of Hemifacial Spasm

NCT00276315 ↗

Phase 3 Completed 332 enrolled Ipsen
RandomizedParallel-groupSingle-blindTreatment

Summary

To compare the effectiveness and safety of Dysport® with the domestic Botulinum Toxin Type A (manufactured by Lanzhou Biologic Product Institute, P.R. China) for the treatment of hemifacial spasm.

Timeline

Start
2005-12
Primary completion
—
Completion
2007-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin type A Protein / enzyme biologic — —

Indications