Long-Term rIsk, Clinical manaGement and Healthcare Resource Utilization of Stable CAD in Post MI Patients



Status:Terminated
Conditions:Peripheral Vascular Disease, Cardiology, Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:50 - Any
Updated:9/5/2018
Start Date:June 19, 2013
End Date:March 31, 2017

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TIGRIS: Long-Term rIsk, Clinical manaGement and Healthcare Resource Utilization of Stable Coronary Artery dISease in Post Myocardial Infarction Patients

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.

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.

Inclusion Criteria:

- Stable CAD patients aged 50 years or older with documented history of presumed
spontaneous MI with their most recent MI occurring 1 to 3 years prior to enrollment and
have at least 1 of the following risk factors: age ≥ 65 years; diabetes mellitus requiring
medication; documented history of a second prior presumed spontaneous MI (>1 year ago);
documented history of angiographic evidence of multivessel coronary artery disease; chronic
renal dysfunction.

Exclusion Criteria:

- Presence of serious co-morbidities in the opinion of the investigator which may limit
life expectancy (<1 year)

- Current participation in a blinded randomized clinical trial.

- Presence of any condition/circumstance which in the opinion of the investigator could
significantly limit the complete follow up of the patient

- Patients receiving treatment of ticagrelor beyond 12 months, or off label use of
ticagrelor.
We found this trial at
36
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Jackson, TN
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Abington, PA
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Arlington Heights, Illinois 60004
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Arlington Heights, IL
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Auburn, ME
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Bangor, ME
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Buenos Aires,
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Burlington, VT
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Chapel Hill, NC
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Clearwater, FL
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Columbia, MD
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Doylestown, PA
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Durham, NC
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Englewood, IL
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Falls Church, VA
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Houston, TX
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Huntsville, AL
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Jackson, MI
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Lebanon, IN
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Los Angeles, CA
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Manassas, VA
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Manhasset, NY
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Miami, FL
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Minneapolis, MN
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Plano, TX
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Providence, RI
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Sandusky, OH
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Santa Ana, CA
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Sayre, PA
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Ventura, CA
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