An Extension to Assess the Effect of Expanded Dialysis on Patient Reported Symptoms Using LEVIL

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorLondon Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

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

100 Participants
are divided into 1 treatment group