Ignite Creation Date:
2024-05-06 @ 1:40 AM
Last Modification Date:
2024-10-26 @ 11:07 AM
Study NCT ID:
NCT01866904
Status:
TERMINATED
Last Update Posted:
2018-09-04
First Post:
2013-05-29
Brief Title:
Long-Term rIsk Clinical manaGement and Healthcare Resource Utilization of Stable CAD in Post MI Patients
Sponsor:
AstraZeneca
Organization:
AstraZeneca
Study Overview
Official Title:
TIGRIS Long-Term rIsk Clinical manaGement and Healthcare Resource Utilization of Stable Coronary Artery dISease in Post Myocardial Infarction Patients
Status:
TERMINATED
Status Verified Date:
2018-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Study was terminated in order to secure the data quality of the study in terms of follow-up rates and data completeness
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
TIGRIS
Brief Summary:
THis study is intended to provide contemporary data on the burden of disease in patients 1 to 3 years post-MI including a description of patient characteristics current treatment patterns rate of major CV events and healthcare resource utilization in a real world patient population at high atherothrombotic risk
Detailed Description:
TIGRIS is a multinational multi-centre observational prospective longitudinal cohort study which will include stable CAD patients with history of MI 1-3 years ago and high risk of developing atherothrombotic events in a real world setting The follow-up period is 3 years
Patients will undergo clinical assessments and receive standard medical care as determined by the treating physician Patients will not receive experimental intervention or experimental treatment as a consequence of their participation in the study
Patients will undergo clinical assessments and receive standard medical care as determined by the treating physician Patients will not receive experimental intervention or experimental treatment as a consequence of their participation in the study
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