Viewing Study NCT00216411



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Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00216411
Status: COMPLETED
Last Update Posted: 2019-07-29
First Post: 2005-09-13

Brief Title: Effects on Quality of Life Following Dysport Treatment in Post-stroke Spasticity of the Arm
Sponsor: Ipsen
Organization: Ipsen

Study Overview

Official Title: A Prospective Phase IV Multicentre Placebo-controlled Study to Demonstrate Changes in the Quality of Life Following DYSPORT Intramuscular Injection in the Treatment of Upper Limb Spasticity in Adult Post-Stroke Patients
Status: COMPLETED
Status Verified Date: 2019-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The main purpose of this study is to assess the effect on Quality of Life of two cycles of Dysport treatment on post-stroke spasticity of the upper limb The effect of treatment on spasticity and function will also be measured
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None