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

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

July 31, 2005

Primary Completion Date

January 31, 2009

Study Completion Date

April 30, 2009

Conditions
Chronic Plantar Fasciitis
Interventions
BIOLOGICAL

Botulinum toxin type A

Botulinum type A toxin (Dysport®): 200 Units injected at the root of the plantar fascia

DRUG

Placebo

0.9% sodium chloride: 2 ml injected at the root of the plantar fascia

Trial Locations (6)

13353

University Hospital Charite, Campus Virchow, Musculoskeletal Centre, Orthopedic Clinic, Berlin

14089

Orthopedic Practice Biberburg, Berlin

76133

Orthopedic Practice, Karlsruhe

81547

Orthocentre Munich, Munich

92637

Orthopedic Practice, Weiden

Unknown

Klinik für Orthopädie und Rheumatologie, Universitätsklinikum Gießen und Marburg GmbH, Marburg

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Ipsen

INDUSTRY

NCT00447876 - Study to Assess the Efficacy and Safety of Dysport® in the Treatment of Chronic Plantar Fasciitis | Biotech Hunter | Biotech Hunter