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Repeatedly measuring the level of Advanced Glycation Endproducts (AGEs) in the acute phase of a myocardial infarction.

Repeated measurements in patients presenting with ST-segment elevation myocardial infarction of Advanced Glycation Endproducts by skin autofluorescence and serum analysis: A pilot study (STAGE study).

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON28558
Enrollment
40
Registered
2012-09-27
Start date
2012-10-15
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ST-segment elevation myocardial infarction (STEMI), Acute Coronary Syndrome (ACS), myocardinfarct

Interventions

Obtainment of blood samples (these repeated procedures will be in alignment with the standard blood sampling as part of standard diagnostic work-up as much as possible).

Sponsors

Erasmus Medical Center, Rotterdam Prof. Eric Boersma, MSc, PhD, FESC, Professor of clinical epidemiology of cardiovascular diseases.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The following inclusion criteria will be applied (all criteria should apply): 1. Men and women, aged from 18 to 70 years, capable of understanding the study content of and willing to provide written informed consent at admission to the hospital; 2. Diagnosis of STEMI, according to the guidelines of the European Society of Cardiology (ESC) 2008. The diagnosis is defined as a history of chest pain / discomfort lasting for 10 ¨C 20 minutes or more (not responding fully to nitroglycerine) with persistent ST segment elevation and elevated markers of myocardial necrosis. Other causes of chest pain / discomfort must be ruled out by the cardiologist; 3. Symptom duration <6h; 4. Blood is drawn before PCI.

Exclusion criteria

Exclusion criteria: Patients with at least one of the following characteristics will be excluded: 1. Myocardial ischemia precipitated by a condition other than atherosclerotic coronary artery disease; 2. Admission for an ACS and / or interventions < 6 months; 3. Diabetes Mellitus; 4. Other existing heart conditions; 5. Clinically significant renal disturbance (GFR (MDRD) &#8804; 30 mL/min/1.73m2) or known renal disease; 6. Severe inflammatory or current malignant disease; 7. Darkly coloured skin; 8. Auto-immune / connective tissue disease; 9. Aorta dissection; 10. Comatose at admission to the CCU; 11. Undergoing PCI for STEMI as a result of complications during elective procedures.

Design outcomes

Primary

MeasureTime frame
The primary endpoints are serial measurements of a) skin AF by the AGE reader® and b) value of AGEs as measured in serum. Furthermore, cardiac enzymes levels will be assessed repeatedly to determine the area under the curve for estimation of the infarct size.

Contacts

Public ContactN. Buljubasic
n.buljubasic@erasmusmc.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)