Clinical trial

Botulinum Type A Toxin in the Treatment of Lateral Canthal Lines (Crow's Feet)

NCT00247559 · Ipsen, Industry · Completed

Key facts

NCT number NCT00247559
Title Botulinum Type A Toxin in the Treatment of Lateral Canthal Lines (Crow's Feet)
Official title A Phase II, Multi-Centre, Randomised, Double-blind, Dose-Ranging Study Comparing the Efficacy and Safety of a Single Treatment With 15, 30 or 45 Units (Per Eye) of Dysport to Placebo in the Symptomatic Treatment of Lateral Canthal Lines (Crow's Feet)
Lead sponsor Ipsen, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Lateral Canthal Lines
Intervention type Biological
Interventions Botulinum toxin type A
Enrollment 221
Start date May 1, 2004
Primary completion Apr 8, 2005
Completion Apr 8, 2005
First posted Nov 2, 2005
Last update posted Nov 22, 2019
Countries France, Germany, United Kingdom

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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