Safety of and Tolerability to a Sodium-free Peritoneal Dialysis Solution
Chronic Kidney Diseases
About this trial
This is an interventional treatment trial for Chronic Kidney Diseases
Eligibility Criteria
Inclusion Criteria: Patients covered by the Mexican Social Security Department. Adults over the age of eighteen. Patients with chronic kidney failure undergoing replacement therapy with peritoneal dialysis. Patients with a functional peritoneal dialysis catheter. Patients undergoing peritoneal dialysis that was stable in the most recent month (ongoing peritoneal dialysis as an outpatient or ongoing cyclic peritoneal dialysis) Patients who wish to participate and who sign the informed consent. If the peritoneal dialysis catheter and the transfer line are compatible with the peritoneal dialysis bag that has a simple luer male connector. If treating doctors consider their patient to be clinically euvolemic. If patients have undergone a peritoneal equilibrium test and their dialysis prescription has not been changed since the test was carried out Exclusion criteria: Diabetes mellitus type 1 or uncontrolled diabetes (a1c hemoglobin greater than 8%). Active infection. Serum sodium prior to the study less than 130 mmol/l. Serum bicarbonate prior to the study less than 18 mmol/l. Patients who have been prescribed standard peritoneal dialysis who only use solutions with the lowest amount of dextrose Hemoglobin less than 8 g/dl. Active bleeding. Patients prescribed peritoneal dialysis who use a 4.25% dextrose solution at least once a day. Patients with a membrane defect or mechanical defect. Diastolic dysfunction with an increase in filling pressure according to the echocardiogram. Patients with active or suspected peritonitis according to the clinical criterion or their treating doctor.
Sites / Locations
- Hospital de Cardiología, Centro Médico Nacional Siglo XXIRecruiting
Arms of the Study
Arm 1
Experimental
30% icodextrin and 10% dextrose
Dwell time of 24 hours using a 500 ml sodium-free peritoneal dialysis solution based on 30% icodextrin and 10% dextrose