Potassium Containing Salt-Substitute in Hemodialysis-Dependent End Stage Kidney Disease
Launched by NYU LANGONE HEALTH · Sep 23, 2022
Trial Information
Current as of July 28, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at the effects of a potassium-containing salt substitute in people with end-stage kidney disease who are on hemodialysis, which is a treatment that helps filter waste from the blood. Sixteen participants will take a potassium salt substitute for 16 days and then standard table salt for another 16 days, with a break in between. The researchers will measure potassium levels and other health indicators throughout the study to see how the salt substitute affects their potassium levels and overall well-being.
To participate, individuals must be at least 21 years old, currently receiving outpatient hemodialysis, and have a negative pregnancy test if they are women of childbearing age. Some people may not be eligible, such as those who have severe potassium levels, certain health conditions, or who have not been regularly attending their hemodialysis sessions. If you decide to join this trial, you can expect to provide information about your diet and health during the study, and you will be closely monitored by the research team.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Receiving outpatient maintenance HD therapy.
- • 2. Age ≥ 21 years.
- • 3. Negative serum pregnancy test for women of child-bearing capacity. Childbearing capacity will be defined by report of menstruation within ≤ 6 months.
- Exclusion Criteria:
- • 1. Currently incarcerated.
- • 2. Insufficient capacity for informed consent.
- • 3. Non-hemolyzed serum potassium concentration \>6.0 mEq/L within ≤30 days.
- • 4. Unscheduled HD for hyperkalemia within ≤30 days.
- • 5. Attendance at ≤10 of last 13 scheduled OP HD sessions.
- • 6. Co-habiting family member with known hyperkalemia.
- • 7. Co-habiting family with ≥stage 3b chronic kidney disease or chronic kidney disease of unknown severity.
- • 8. Hemoglobin \< 8.0 mg/dL.
- • 9. Use of other potassium supplements.
About Nyu Langone Health
NYU Langone Health is a premier academic medical center located in New York City, renowned for its commitment to advancing healthcare through innovative research and clinical excellence. As a leading sponsor of clinical trials, NYU Langone Health integrates cutting-edge scientific inquiry with patient-centered care, striving to develop new therapies and improve health outcomes across a wide range of medical conditions. The institution is dedicated to fostering collaboration among researchers, clinicians, and patients, ensuring rigorous adherence to ethical standards and regulatory guidelines in all clinical research initiatives. By leveraging its extensive resources and expertise, NYU Langone Health aims to contribute significantly to the advancement of medical knowledge and the enhancement of patient care.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New York, New York, United States
Patients applied
Trial Officials
David Charytan, MD MSc
Principal Investigator
NYU Langone Medical Center
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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