About this trial
The goal of this clinical trial is to find out if using a citrate-based dialysate with added magnesium during hemodialysis can help slow down or prevent the hardening of blood vessels (vascular calcification) in adults on long-term dialysis.
The main questions the study will try to answer are:
Does citrate-based dialysate with magnesium improve the blood's ability to prevent calcium buildup (measured by a test called T50) compared to acetate-based dialysate?
Does it modify magnesium, calcium and parathyroid hormone (PTH) levels in the blood?
Does it lower the chances of heart problems or death?
Researchers will compare two groups: one will receive acetate-based dialysate, and the other will receive citrate-based dialysate with magnesium.
Participants will:
Receive one of the two types of dialysate during their regular hemodialysis sessions for 12 months
Have regular blood tests
Be monitored for any heart problems and for overall health during the study
Eligibility criteria
Qualifiers
Adults (≥18 years old) on maintenance hemodialysis for more than 3 months
Clinically stable patients with a well-functioning vascular access
Residual urine output ≤ 250 mL/day
Able and willing to provide written informed consent
Disqualifiers
Known allergy or intolerance to any component of the dialysates
Active malignancy or infectious/inflammatory disease
Planned living donor kidney transplant before study completion
Current treatment with vitamin K antagonists (coumarins)
Trial design
Treatments tested in this trial
- Citrate dialysate with magensium supplementation
- Acetate dialysate