About this trial
This study aims to assess whether two blood markers - C-reactive protein (CRP) and D-dimer - can help predict cardiovascular complications in patients undergoing regular hemodialysis. Cardiovascular disease is a common and serious problem in dialysis patients, and early detection is important.
the study will include 100 adult patients from the Hemodialysis Unit at Assiut University Hospital. Participants will be divided into two groups: those with and those without known heart disease. Each participant will have a one-time blood test to measure CRP and D-dimer levels. In addition, an electrocardiogram (ECG) will be done once to check for signs of heart problems.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults aged ≥18 years
Disqualifiers
Acute or recent infection (within the past 4 weeks)
Trial population
Hemodialysis patients treated at the Hemodialysis Unit of Assiut University Hospital, including those with and without documented cardiovascular disease.
Trial design
Cohort
Cross-sectional
Treatments tested in this trial
C-Reactive Protein (CRP) Test
Diagnostic testBlood samples will be collected once from all participants to measure CRP levels
D-dimer Test
Diagnostic testD-dimer levels will be assessed once to evaluate thrombotic risk.
Electrocardiogram (ECG)
Diagnostic testA standard 12-lead ECG will be performed once per participant to assess cardiovascular status
Treatment groups
Trial outcomes
Primary outcomes
Serum CRP level among hemodialysis patients
To assess the level of serum CRP in hemodialysis patients with and without cardiovascular disease and compare values between the two groups to explore possible associations
Plasma D-dimer level among hemodialysis patients
To assess the level of plasma D-dimer in hemodialysis patients with and without cardiovascular disease and compare values between the two groups to explore possible associations.
Secondary outcomes
Presence of cardiovascular abnormalities on ECG
To assess cardiovascular status of hemodialysis patients using a standard 12-lead ECG and record the presence of abnormal findings
Sponsors and contacts
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