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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04034940
Other study ID # OxiSTEMI01
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 2019
Est. completion date August 2020

Study information

Verified date July 2019
Source Grigore T. Popa University of Medicine and Pharmacy
Contact Razan Al Namat, MD, PhD stud
Phone 0040757205114
Email dr.razan_romania@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators intend to evaluate Oxidative Stress biomarkers through a. Catalase Activity Assay; b. Lipid Peroxidation Assay; c. SOD Assay; d. Total Antioxidant Capacity Assay; e. Glutathione Peroxidase at patients with acute myocardial infarction STEMI referred for primary PCI; The investigators also aim to evaluate cardiac necrosis by measuring Heart Fatty Acid Binding Protein (H-FABP), TnI, CK, CK-MB, LDH and AST in these patients with acute myocardial infarction referred for primary PCI; Also, the investigators intend to evaluate body composition through bioimpedance spectroscopy (BCM - Fresenius Care) at the moment of admission.

The investigators aim to fully characterise these patients through oxidative millieu, hFABP and make correlations with LVEF dysfunction.


Description:

Gathered data:

- Descriptive general demographic data;

- Previous pathologies (ischemic heart disease, peripheral arterial disease, stroke, heart failure, previous percutaneous coronary interventions, coronary artery bypass grafting - CABG, known renal disease);

- Cardiovascular risk factors (age, weight, height, abdominal perimeter, body mass index, smoking, sedentariness, diabetes, hypertension, dyslipidaemia);

- Oxidative Stress biomarkers: Catalase Activity Assay; Lipid Peroxidation Assay; SOD Assay; Total Antioxidant Capacity Assay; Glutathione ;

- Cardiac necrosis markers: Heart Fatty Acid Binding Protein (H-FABP), TnI, CK, CK-MB, LDH and OGT;

- Routine biological data;

- Metabolic data (obtained from two body composition monitoring evaluations - before and 12 hours after coronary intervention) - body water, body fat tissue;

- Information regarding primary PCI (less than 12 hours of ischemic symptoms);

- Coronarographic details, type of used stent, periprocedural specific complications, final TIMI - thrombolysis in myocardial infarction - flow);

- Echocardiography at admission (LVEF);

- Measurement of arterial stiffness through Sphigmocore pulsed-wave-velocity (24 hrs post-procedural, 2 velocities: carotid - femoral and carotid - radial);

- Calculating of cardiovascular risk scores: Syntax Score, Framingham score, ASSIGN score, QRISK2 score, PROCAM score, CRUSADE score, GRACE score, CHADS VASc score, MESA score, ASCVD score, Hamilton Depression Rating Scale (HAM-D), Hamilton Rating Scale for Anxiety;

- In-hospital and one month follow-up MACE.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date August 2020
Est. primary completion date July 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adults with ST elevation Myocardial Infarction (<12h) diagnostic confirmed;

- Included in the Romanian National Programme of Primary Percutaneous Revascularisation (for who the Guidelines recommend primary PCI);

Exclusion Criteria:

- Patients who do not sign informed consent for primary PCI

Study Design


Intervention

Other:
Dosing Oxidative stress biomarkers & hFABP in STEMI pPCI patients
Dosing oxidative stress biomarkers and hFABP in STEMI pPCI

Locations

Country Name City State
Romania Cardiovascular Diseases Institute Iasi Iasi Iasi

Sponsors (2)

Lead Sponsor Collaborator
Grigore T. Popa University of Medicine and Pharmacy Cardiovascular Diseases Institute IASI, Romania

Country where clinical trial is conducted

Romania, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oxidative Stress status in Acute Myocardial Infarction Patients undergoing primary PCI Assessment of oxidative stress status by measuring Catalase Activity Assay; Lipid Peroxidation Assay; SOD Assay; Total Antioxidant Capacity Assay; Glutathione Peroxidase. 1 year
Primary 2. Cardiac necrosis status in Acute Myocardial Infarction Patients undergoing primary PCI. Assessment of cardiac necrosis by measuring Heart Fatty Acid Binding Protein (H-FABP), TnI, CK, CK-MB, LDH and AST 1 year
Secondary Hydation Status in Acute Myocardial Infarction Patients undergoing primary PCI. Assessment of hydration status through body composition monitoring BCM. 1 year
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