The Reducing Adverse Outcomes in Dialysis by Adjusting the pRescription for Dialysate Potassium Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21+
SponsorNYU Langone Health

About this trial

This will be a randomized controlled pilot trial comparing usual care to a precision approach to dialysis potassium prescribing. The precision approach will incorporate point of care testing of blood potassium concentration prior to each dialysis session and adjustment of the dialysate K prescription with a blood-dialysate K gradient minimization strategy (PKRxHD).

Eligibility criteria

Qualifiers

Undergoing in-center, 3x/weekly HD for treatment of end-stage kidney disease (ESKD) for at least 90 days

Age at least 21 years

Prescribed HD time up to 15 hours/ week

Disqualifiers

Incarcerated

Life expectancy of 1 year or less

Kidney transplant, transition to home dialysis, or transfer to non-participating HD unit anticipated within 6 months or less

Cognitive condition that precludes consent

Trial design

Treatments tested in this trial

  • PKRxHD
  • Dialysis

Treatment groups

120 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

NYU Langone Health

Lead sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborator