Heart Failure Clinical Trial
Official title:
The Use of miRNA Detection for Diagnostics of Cardiovascular Diseases
Verified date | February 2023 |
Source | University Hospital Ostrava |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of the study is to determine the analytical characteristics of the microRNA enzymatic immunoassay (miREIA) method and to determine various relations among miRNA biomarkers and heart failure (HF) with reduced ejection fraction(HFrEF). The investigators assume that there are correlations between levels of selected miRNA and HFrEF. These correlations provide information to formulate pathophysiological conclusions, which will significantly contribute to early diagnostics and also the treatment of this disease.
Status | Active, not recruiting |
Enrollment | 200 |
Est. completion date | December 31, 2023 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 99 Years |
Eligibility | Inclusion criteria (patient group): - left ventricle ejection fraction (EF LV) equal or less than 40% - age between 18-80 years Inclusion criteria (control group): - normal EF LV (left ventricular ejection fraction) - no structural cardiac abnormalities - age between 18-80 years. Exclusion criteria: - recent myocardial infarction - recent percutaneous coronary intervention (PCI) - recent decompensation of chronic heart failure - chronic kidney disease with need for haemodialysis - creatin level over 450 umol/l - signs of acute or chronic inflammation with CRP (C-reactive protein) over 20 mg/l - patient with a known tumour - history of cardiovascular disease - diabetes mellitus - severe liver and kidney disease - BNP (brain natriuretic peptide) > 250 pg/ml or NTproBNP > 500 pg/ml for males and 750 pg/ml for females - signs of acute or chronic inflammation with CRP over 20 mg/l |
Country | Name | City | State |
---|---|---|---|
Czechia | University Hospital Ostrava | Ostrava-Poruba | Czech Republic |
Lead Sponsor | Collaborator |
---|---|
University Hospital Ostrava |
Czechia,
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* Note: There are 22 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Levels of miRNA (in pmol/L) | Full blood samples will be taken in both groups after period of clinically stable state and analyzed for levels of miRNA(hsa-miR-21-5p; hsa-miR-23a-3p; hsa-miR-142-5p; hsa-miR-126-3p) with biochemical microRNA enzymatic immunoassay. Measured levels of listed four miRNAs will be provided pmol/L.
These levels will be statistically analyzed and compared between patient and control group. |
43 months | |
Secondary | Correlation between miRNA levels and 1-year mortality and risk of rehospitalization | We will examine levels of miRNA in corelation to 1-year mortality and risk of rehospitalization acquired from Czech national registry (UZIS). | 43 months |
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