Viewing Study NCT01996761


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Study NCT ID: NCT01996761
Status: COMPLETED
Last Update Posted: 2016-05-11
First Post: 2013-11-05
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Effects of Cerebrolysin on Motor Recovery in Patients With Subacute Stroke
Sponsor: Samsung Medical Center
Organization:

Study Overview

Official Title: Effects of Cerebrolysin on Motor Recovery in Patients With Subacute Stroke
Status: COMPLETED
Status Verified Date: 2016-05
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: E-COMPASS
Brief Summary: This study, E-COMPASS is a phase IV clinical trial designed as a multicenter, randomized, double-blind, placebo-controlled, parallel-group study. This study will enroll 75 subacute stroke patients with unilateral motor dysfunction. Primary objective is to demonstrate the efficacy of porcine brain peptide to improve motor recovery measured by the improvement ratio of Fugl-Meyer assessment ((score of FMA after 3 weeks - score of FMA at baseline) / score of FMA at baseline) in patients with subacute stroke.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: