Assessment of Biomarkers for Diagnosis in Geriatric Patients
NCT ID: NCT01370395
Last Updated: 2012-10-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
250 participants
OBSERVATIONAL
2011-01-31
2013-12-31
Brief Summary
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Detailed Description
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At admission, patient history, physical examination, prior medications, vital signs including heart rate, blood pressure, body temperature, and all comorbidities will be recorded by a physician. Blood samples will be collected at the time of presentation. Determination of regular laboratory values together with very low circulating troponin T, copeptin, MR-pro-adrenomedullin, ANP and endothelin-1 levels will be measured. An electrocardiogram will be taken in all patients at admission. An echocardiography measuring the function of the heart valves, left ventricular diameters, ejection fraction (LV-EF), and diastolic function will be performed in all patients by a cardiologist in order to differentiate other mechanisms for the release of troponin. According to the result of the echocardiographic exam, the patients will be divided into subgroups with (LV-EF\>=55%) and without preserved ejection fraction (LV-EF\<55%).
Objectives:
1. To investigate the incidence of acute coronary syndromes in geriatric patients by measurement of very low circulating troponin T and copeptin levels.
2. To determine cardiovascular events, including cardiovascular death, fatal and nonfatal heart failure, and fatal and nonfatal acute myocardial infarction, of these patients during 24 months.
3. To analyze the relationship between very low circulating troponin T and cardiovascular events in these patients.
4. To analyze risk factors in geriatric patients with elevated troponin T for cardiovascular events.
5. To analyze whether the combined measurement of troponin T and copeptin or other markers improves the sensitivity for identification of acute coronary syndromes in geriatric patients.
Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Left ventricular function
According to the result of the echocardiographic exam, the patients will be divided into subgroups with (LV-EF\>=55%) and without preserved ejection fraction (LV-EF\<55%).
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Signed informed consent
Exclusion Criteria
* ST-segment elevation myocardial infarction
* Heart valve defects with need for surgical intervention
* Coronary bypass surgery or percutaneous transluminal angioplasty within the last 3 months
* Planned elective coronary revascularization
* Serum creatinine\> 2.0 mg / dl (177 µmol / liter)
* Serum potassium\> 5.5 mmol / l
* Limited survival probability within the next 3 months
70 Years
ALL
No
Sponsors
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Klinikum Nürnberg
OTHER
University of Erlangen-Nürnberg Medical School
OTHER
Responsible Party
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Philipp Bahrmann
MD
Principal Investigators
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Philipp Bahrmann, MD
Role: PRINCIPAL_INVESTIGATOR
Department of Internal Medicine II-2, Chair of Internal Medicine V, Institute for Biomedicine of Ageing, Friedrich-Alexander-Universität Erlangen-Nürnberg
Locations
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Klinikum
Nuremberg, , Germany
Countries
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References
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Bahrmann P, Christ M, Bahrmann A, Rittger H, Heppner HJ, Achenbach S, Bertsch T, Sieber CC. A 3-hour diagnostic algorithm for non-ST-elevation myocardial infarction using high-sensitivity cardiac troponin T in unselected older patients presenting to the emergency department. J Am Med Dir Assoc. 2013 Jun;14(6):409-16. doi: 10.1016/j.jamda.2012.12.005. Epub 2013 Jan 30.
Bahrmann P, Bahrmann A, Breithardt OA, Daniel WG, Christ M, Sieber CC, Bertsch T. Additional diagnostic and prognostic value of copeptin ultra-sensitive for diagnosis of non-ST-elevation myocardial infarction in older patients presenting to the emergency department. Clin Chem Lab Med. 2013 Jun;51(6):1307-19. doi: 10.1515/cclm-2012-0401.
Other Identifiers
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BOSCH1
Identifier Type: -
Identifier Source: org_study_id