TURKish Acute Myocardial Infarction Registry
-
- STATUS
- Recruiting
-
- participants needed
- 1930
-
- sponsor
- Turkish Society of Cardiology
Summary
There is no up-to-date information regarding presentation, management and clinical course of
patients with
Description
Background: There is no up-to-date information regarding presentation, management and
clinical course of patients with
Methods: TURKMI study, as a nation-wide registry, will be conducted in 50 percutaneous
coronary intervention -capable centres selected from each EuroStat NUTS region in Turkey
according to their population sampling weight, prioritizing the volume of hospital in each
region. All consecutive patients with
The first step of the study has cross-sectional design in which baseline information such as symptoms, risk factors, time periods at each step from symptom onset to revascularization, way of arrival to hospital, biochemical analysis and in-hospital management and outcome will be assessed. The second step has a cohort characteristics in which enrolled patients will be followed-up up to 2 years. Follow-up visits will be conducted at 1st, 6th, 12th and 24th months, and predictors and risk of cardiovascular events, and implementation of guidelines will be assessed as secondary outcomes.
Conclusion: The national TURKMI registry is expected to provide important information to improve the national policy of the diagnosis, management and outcomes of MI in Turkey
Details
Condition |
|
---|---|
Age | 18years - 100years |
Treatment | No intervention |
Clinical Study Identifier | NCT04241770 |
Sponsor | Turkish Society of Cardiology |
Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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