Post Marketing Surveillance Study of Dysport

Ipsen

Status: Completed

Conditions: Cerebrovascular Accident; Cervical Dystonia; Equinus Deformity; Spasmodic Torticollis; Blepharospasm; Cerebral Palsy; Muscle Spasticity; Facial Hyperdynamic Lines; Hemifacial Spasm

Study type: Observational

Funder types: Industry

Identifiers

NCT00210431

Y-47-52120-093

Details and patient eligibility

About

The purpose of this study is to provide further information regarding the risks and benefits of Dysport in marketed indications.

Enrollment: 783 patients

Sex: All

Ages: 2+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• adult or child over the age of 2 years
• scheduled to receive Dysport as per their normal treatment practice, and in conformance with their country's Summary of Product Characteristics

Exclusion criteria

• history of hypersensitivity to Dysport or drugs with a similar chemical structure
• treatment with any other investigational drug within the last 30 days before survey entry