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

Chronic Plantar Fasciitis Clinical Trial

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

Status Completed

Clinical Trial Summary

This study will investigate the hypothesis that the analgesic effect of a single injection of Dysport (200 MU) induces a significant reduction of symptoms in chronic cases of plantar fasciitis.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00447876
Study type	Interventional
Source	Ipsen
Contact
Status	Completed
Phase	Phase 2/Phase 3
Start date	July 2005
Completion date	April 2009

View Details

See also
Status	Clinical Trial	Phase
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Recruiting	`NCT01614223` - Autologous Conditioned Plasma (ACP) for Patients With Plantar Fasciitis	N/A
Completed	`NCT03255655` - Intense Therapeutic Ultrasound - Treatment for Chronic Plantar Fascia Musculoskeletal Pain Reduction	N/A
Completed	`NCT06348017` - Frequency of Neuropathic Pain in Patients With Plantar Fasciitis
Recruiting	`NCT05868577` - Infracalcaneal Peppering Injection Technique for Chronic Plantar Fasciitis	Phase 1
Recruiting	`NCT03938896` - PRP IN Planter Fascitis	N/A
Recruiting	`NCT05032300` - Shear Wave Elastography Technology to Evaluate the Efficacy of ESW in the Treatment of Patients With Chronic Plantar Fasciitis	N/A
Completed	`NCT05754697` - IASTM Versus PRT in Patients With Chronic PF	N/A
Active, not recruiting	`NCT05162144` - Proximal Medial Gastriocnemius Recession for Chronic Plantar Fasciitis	N/A