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Improving Care for Peritoneal Dialysis Patients With the CKD-PD App

NCT04797195 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 208

Last updated 2025-02-11

Study results available
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Summary

Managing the hydration status in patients undergoing peritoneal dialysis (PD) is a key task for nephrologists in Thailand that is made difficult due to lack of timely access to hydration metrics including weight, blood pressure, and ultrafiltration volume. This research project aims to improve the monitoring of hydration status in PD patients from a bimonthly, in-clinic review of a handwritten log-book to a smart phone based app (CKD-PD) with digitized data that allows for near real time monitoring hydration abnormalities, thereby creating the opportunity for earlier treatment of overhydration. The investigators hypothesize that use of the CKD-PD will improve early treatment of overhydration, and potentially reduce the incidence of complications, hospitalizations, and mortality in PD patients.

Conditions

  • Kidney Failure, Chronic
  • Peritoneal Dialysis Complication

Interventions

OTHER

CKD-PD app with home monitoring equipment

use home monitoring equipment to measure blood pressure, body weight, and dialysate fluid volume and record in CKD-PD app

Sponsors & Collaborators

  • Khon Kaen University

    collaborator OTHER

  • Fogarty International Center of the National Institute of Health

    collaborator NIH

  • Massachusetts General Hospital

    lead OTHER

Principal Investigators

  • Katharine E Morley, MD, MPH · Massachusetts General Hospital

  • Sirirat Anutrakulchai, MD PhD · Srinagarind Hospital, Khon Kaen University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-12-13
Primary Completion
2023-04-30
Completion
2023-04-30

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04797195 on ClinicalTrials.gov