Actively Recruiting

Age: 21Years +
All Genders
NCT07059962

Sensor-based Congestion ALert for Events in Peritoneal Dialysis (SCALE-PD)

Led by Bodyport Inc. · Updated on 2026-03-18

125

Participants Needed

4

Research Sites

37 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Sensor-based Congestion ALert for Events in Peritoneal Dialysis (SCALE-PD)

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 21 years or older
  • Able to speak and read English, or speak and read Spanish with a caregiver or family member who speaks English and can assist
  • Able to stand on two bare feet unassisted
  • Receiving automated peritoneal dialysis for the treatment of end-stage kidney disease
  • Followed on the Vantive Sharesource Remote Patient Management Platform
Not Eligible

You will not qualify if you...

  • Currently undergoing or planning to undergo hemodialysis in the next 12 months
  • Have a life expectancy of less than 12 months
  • Are pregnant or plan to become pregnant during the next 12 months
  • Weigh greater than 375 pounds
  • Planned kidney transplant within the next 12 months
  • Have an implanted neurostimulator system

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Desert Cities Dialysis

Victorville, California, United States, 92395

Actively Recruiting

2

Southeastern Clinical Research Institute

Augusta, Georgia, United States, 30904

Actively Recruiting

3

Northwestern University

Chicago, Illinois, United States, 60611

Actively Recruiting

4

Seven Oaks General Hospital

Winnipeg, Manitoba, Canada, R2V 3M3

Actively Recruiting

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Research Team

C

Corey Centen

CONTACT

D

Dorothy Kwok

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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