Ignite Creation Date:
2024-05-05 @ 5:15 PM
Last Modification Date:
2024-10-26 @ 9:29 AM
Study NCT ID:
NCT00412867
Status:
COMPLETED
Last Update Posted:
2018-01-19
First Post:
2006-12-17
Brief Title:
Post-marketing Clinical Study of Alteplase for Acute Ischemic Stroke Japan Alteplase Clinical Trial ⅡJ-ACT Ⅱ
Sponsor:
Mitsubishi Tanabe Pharma Corporation
Organization:
Mitsubishi Tanabe Pharma Corporation
Study Overview
Official Title:
Post-marketing Clinical Study of Alteplase for Acute Ischemic Stroke Phase 4
Status:
COMPLETED
Status Verified Date:
2017-12
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 purpose of this study is to confirm the efficacy and safety of intravenously administered alteplase in patients with acute ischemic stroke based on the rate of recanalization assessed by magnetic resonance angiography MRA the rate of patients with a modified Rankin Scale mRS score of 0-1 and the incidence of symptomatic intracranial hemorrhage sICH in comparison with the data reported in the current literature
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