Clinical trial

Study to Assess the Efficacy and Safety of Dysport® in the Treatment of Chronic…

NCT00447876 · Ipsen, Industry · Completed

Key facts

NCT number NCT00447876
Title Study to Assess the Efficacy and Safety of Dysport® in the Treatment of Chronic Plantar Fasciitis
Official title Double-blind, Placebo-controlled, Randomised, Multicentre Study on the Efficacy and Safety of a Single Injection of Botulinum Toxin A (200 Units Dysport®) in the Treatment of Chronic Plantar Fasciitis
Lead sponsor Ipsen, Industry
Status Completed
Phase Phase 2/Phase 3
Study type Interventional
Conditions Chronic Plantar Fasciitis
Intervention type Biological, Drug
Interventions Botulinum toxin type A, Placebo
Enrollment 40
Start date Jul 1, 2005
Primary completion Jan 1, 2009
Completion Apr 1, 2009
First posted Mar 15, 2007
Last update posted Nov 22, 2019
Countries Germany

At a glance

  • 1–9 Study sites
  • Yes 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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