About this trial
Investigators know that many patients who are on dialysis suffer from burden of unwanted symptoms, which can affect quality of life. The understanding and treatment of symptom burden by healthcare providers is limited and should be recognized as a high priority in the care of the dialysis population. In this study, the investigators will be assessing symptom burden using the London Evaluation of Illness "LEVIL," an application based platform where patients self-report their symptoms with one to three hemodialysis treatments per week for 28 weeks. The investigators would like to compare the currently available dialyzer with a new dialyzer that is capable of removing solutes of higher molecular weight that may or may not cause patients to experience symptoms related to increased amounts of toxins in their blood.
Eligibility criteria
Qualifiers
Conventional thrice weekly HD schedule
Must be on chronic hemodialysis for at least 3 months
Age ≥18 years
Willing and able to give informed consent
Disqualifiers
Active infection (may enroll once infection is cleared)
Patients receiving daily hemodialysis treatment
Patients currently receiving Hemodiafiltration (HDF), Hemofiltration (HF) or Isolated ultrafiltration (ISO UF) more than once in three months
Visual impairment
Trial design
Treatments tested in this trial
- Theranova Dialyzer
Treatment groups
Sponsors and collaborators
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead sponsor
Baxter Healthcare Corporation
Collaborator