To Document the Effectiveness of BoNT-A Injection in Adult Subjects With Upper Limb Spasticity Following Stroke (ULIS2)

Ipsen

Status: Completed

Conditions: Muscle Spasticity

Study type: Observational

Funder types: Industry

Identifiers

NCT01020500

Y-79-52120-138

Details and patient eligibility

About

The purpose of the study is to assess the responder rate as defined by the achievement of the primary goal from the Goal Attainment Scale following one BoNT-A injection cycle in accordance with routine practices.

Enrollment: 469 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Upper limb spasticity following stroke
• At least a 12-week interval between the last injection (BoNT-A or BoNT-B) and inclusion
• Decision already been agreed to inject BoNT-A
• Agreement with the subject on goal setting

Exclusion criteria

• Contraindications to any BoNT-A preparations