Screen CardRen - A Cross-sectional Observational Cohort Study
- Conditions
- Heart FailureChronic Kidney Diseases
- Registration Number
- NCT06272578
- Lead Sponsor
- Charite University, Berlin, Germany
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 400
Inclusion Criteria:<br><br>Chronic Kidney Disease, stages G1-G4, AND<br><br> - Estimated glomerular filtration rate (eGFR) as determined by the 2009 CKD-EPI Cr<br> equation = 60 ml/min/1.73m², if UACR =30 mg/g (=3 mg/mmol) OR<br><br> - eGFR according to CKD-EPI 2009 Cr equation < 60 ml/min/1.73m², but > 15<br> ml/min/1.73m²<br><br>Diabetes mellitus type 2 OR<br><br> - Pathological findings in oral glucose tolerance test (= 200 mg/dl (2h)) OR<br><br> - documented HbA1c = 6.5 % OR<br><br> - Intake of any antidiabetic medication (in case of previously established diagnosis<br> of Diabetes mellitus type 2) OR<br><br> - Fasting blood glucose = 126 mg/dl<br><br>Arterial Hypertension Grade = 1 OR<br><br> - Blood pressure of = 140/90 mmHg, defined according to the 2018 ESC guidelines on<br> arterial hypertension (Williams) OR<br><br> - Intake of antihypertensive drugs<br><br>Hypercholesterolemia OR<br><br> - LDL-cholesterol > 130mg/dl OR<br><br> - Intake of a lipid-lowering medication initiated to treat dyslipoptroteinemia<br><br>Exclusion Criteria:<br><br>History of acute kidney injury > stage 1 according to KDIGO criteria in the two weeks<br>prior to study visit<br><br> - Chronic kidney disease Stage 5 (end-stage renal disease)<br><br> - Previous diagnosis of chronic heart failure<br><br> - Acute myocardial infarction in the past 30 days prior to study visit<br><br> - Stroke in the past 30 days prior to study visit<br><br> - Known congenital heart disease<br><br> - Previous diagnosis of a specific cardiomyopathy, infiltrative cardiac disease,<br> pericardial constriction, sarcoidosis, amyloidosis and other storage diseases<br><br> - Implanted cardiac devices, such as pacemakers, implantable<br> cardioverter-defibrillators, cardiac resynchronization devices<br><br> - Implanted mechanical valve prosthesis<br><br> - Inability to give informed consent<br><br> - Lack of health insurance<br><br> - Organ transplanted<br><br> - Intake of immunosuppressive medication<br><br> - Major surgery in the 6 months before study visit, such as cardiac bypass surgery or<br> valve replacement surgery (thoracotomy), major vascular surgery (such as replacement<br> of aortic root, ascending part, aortic arch or any part of the abdominal aorta),<br> major abdominal surgery (e.g. Whipple procedure, colorectal resection, gastrectomy<br> and others) or limb amputation
Not provided
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method prevalence of significant asymptomatic cardiac structural abnormalities and cardiac dysfunction;Proteomic analysis
- Secondary Outcome Measures
Name Time Method Duration of echocardiographic examination;Time saved by portable echocardiography and automated image analysis;Image quality of cart-based vs. portable echo images