Sensor-based Congestion ALert for Events in Peritoneal Dialysis (SCALE-PD)
To explore the use of the Bodyport Cardiac Scale in predicting worsening of events due to fluid overload in patients with kidney disease on peritoneal dialysis.
| Condition(s) | Kidney Disease, Peritoneal Dialysis (PD), End Stage Kidney Disease (ESRD) |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | To explore the use of the Bodyport Cardiac Scale in predicting worsening of events due to fluid overload in patients with kidney disease on peritoneal dialysis. |
| Who can participate | Inclusion Criteria: 1. Age 21 years or older 2. Able to speak and read English, or able to speak and read Spanish and has a caregiver or family member who speaks English and can provide assistance 3. Able to stand on two bare feet unassisted 4. Receiving automated peritoneal dialysis for the treatment of ESKD 5. Followed on the Vantive Sharesource Remote Patient Management Platform Exclusion Criteria: 1. Undergoing or plan to undergo hemodialysis in the next 12 months 2. Have a life expectancy of less than 12 months 3. Are pregnant or plan to become pregnant during the next 12 months 4. Weigh greater than 375 lbs 5. Planned kidney transplant within the next 12 months 6. Have an implanted neurostimulator system |
| Ages | 21 Years |
| Sex | All |
| Lead sponsor | Bodyport Inc. |
| Locations | Victorville, California, United States; Augusta, Georgia, United States; Chicago, Illinois, United States; Winnipeg, Manitoba, Canada |
| Start date | 2025-09-09 |
| NCT ID | NCT07059962 |
| Official listing | https://clinicaltrials.gov/study/NCT07059962 |