- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04578964
Determining the Age of First Acute Coronary Syndrome
Determining the Cardiovascular Risk Factors Affecting the Age of First Acute Coronary Syndromes
Study Overview
Status
Detailed Description
In the first stage, the first ACS diagnosis of the patients will be tried to be clarified. It will be tried to clarify whether the patients have had ACS before, according to their history, ecg echo and coronary angiography findings. Patients with previous ACS or uncertain ACS diagnosis will not be included in the study.
In the second stage, cardiovascular risk burdens of patients for whom the initial ACS diagnosis is clear will be revealed. Smoking, diabetes mellitus (DM), hypertension (HT), psychological stress, socio-economic status, migration history, cholesterol parameters will be determined. The duration and severity of these risk factors will be determined. In the final model, each risk factor will be examined in detail with its sub-tabs and the effect of each risk factor will be examined separately.
Eventually, a model will be developed that allows predicting the first ACS age. The shortcomings of this model and the narrow scope of the definition of the population will be determined and the direction will be determined for the studies that improve these points.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Deniz Demirci, MD
- Phone Number: +905056847321
- Email: dddemirci@gmail.com
Study Locations
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-
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Antalya, Turkey
- Recruiting
- Deniz Demirci
-
Contact:
- Deniz Demirci, MD
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult patients with the diagnosis of the first acute coronary syndrome
Exclusion Criteria:
- Previous cardiovascular disease
- Chronic renal disease,
- Chronic obstructive pulmonary disease,
- Malignancy,
- Regularly use of statins, antiplatelets or anticoagulants,
- Situations where oral communication cannot be established with the patient
- Situations when coronary angiography (CAG) could not be performed .
- Patients with findings that might be related to previous MI on electrocardiography (ECG) or echocardiography and total occlusion other than 'culprit' lesion and no critical stenosis on CAG
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Determining the effect of cardiovascular risk factors on the mean age of the first acute coronary syndrome
Time Frame: 10 years
|
Detection of the effect of gender, smoking, obesity, diabetes, hypertension, psychological stress, socioeconomic status, migration, dyslipidemia on the age of first acute coronary syndrome episode.
|
10 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Determining the effect of obesity on the mean age of the first acute coronary syndrome
Time Frame: 6 years
|
Grouping will be made to obesity degree (Normal, overweight, obesity severe obesity).
The first ACS average age of these groups will be compared.
Risk factors affecting this average age will not be revealed by linear regression model.
|
6 years
|
|
Determining the effect of migration on the mean age of the first acute coronary syndrome.
Time Frame: 6 years
|
Do the patients live in the city where they were born.
It will be determined whether he migrated from another city.
If there is a migration situation, the reasons will be determined.
The migration direction will be determined according to the regions.
The impact of migration and migration direction on the first ACS age will be determined.
|
6 years
|
|
Model for calculating the acute coronary syndrome age
Time Frame: 8 years
|
Develop a model that calculates the estimated age of ACS on the basis of cardiovascular risk factors.
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8 years
|
Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2014-097
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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