Examine the Epidemiology and Outcomes of Transitions From PD-to-HD in Canada (UPLIFT-PD CORR)

March 13, 2026 updated by: Annie-Claire Nadeau-Fredette, Ciusss de L'Est de l'Île de Montréal

Understand, Plan and Improve Care and Wellbeing of Patients at High Risk of Transfer From Peritoneal Dialysis to Hemodialysis, Epidemiology (Phase 1)

Transitions from peritoneal dialysis to hemodialysis are common during kidney replacement therapy and may be associated with adverse outcomes. However, the incidence, predictors, and outcomes of PD-to-HD transitions at a national level remain incompletely characterized.

This study will use Canadian dialysis and hospitalization databases to examine the epidemiology and outcomes of PD-to-HD transitions among adults initiating dialysis in Canada. The study will evaluate transition incidence, predictors, and post-transition outcomes including mortality, transplantation, modality changes, and hospitalizations.

Study Overview

Status

Active, not recruiting

Study Type

Observational

Enrollment (Estimated)

17000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Quebec
      • Montreal, Quebec, Canada, H1T 2M4
        • CIUSSS de l'Est-de-l'ile de Montréal

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Adults initiating dialysis in Canada between 2005 and 2018 who received peritoneal dialysis for at least 30 consecutive days, identified using the Canadian Organ Replacement Register (CORR) and linked administrative databases.

Description

Inclusion Criteria:

  • Adults (≥18 years)
  • Dialysis initiation in Canada between January 1, 2005 and December 31, 2018
  • Peritoneal dialysis duration >30 consecutive days

Exclusion Criteria:

  • Dialysis initiation in Quebec or Manitoba during the study period
  • Dialysis initiation in a foreign country
  • Missing data on initial dialysis modality
  • Pre-emptive kidney transplantation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Patient receiving peritoneal dialysis with transfer to hemodialysis
Adults initiating dialysis in Canada between 2005 and 2018 who received peritoneal dialysis and experience a transfer to hemodialysis for 2 or more consecutive days.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence of transfer from peritoneal dialysis to hemodialysis
Time Frame: From PD initiation until 1-year after PD start Also assessed at from PD initation until 2- and 5-year after PD start.
Measured as cumulative incidence and incidence rate of transitions following initiation of PD and censored at time of death, kidney transplantation, transfer home hemodialysis, or administrative end of follow-up.
From PD initiation until 1-year after PD start Also assessed at from PD initation until 2- and 5-year after PD start.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
All-cause mortality after transfer from peritoneal dialysis to hemodialysis
Time Frame: From first day after transfer up to 1-year post transfert. Also assessed ad 2- and 5-year post transfer
Censored for kidney transplantation, transfer home hemodialysis, return to PD or administrative end of follow-up December 31st, 2018
From first day after transfer up to 1-year post transfert. Also assessed ad 2- and 5-year post transfer
Return to Peritoneal Dialysis
Time Frame: From first day after transfer to HD up to 180-day post transfer. Also measured at 90- and 365-day post transfer.
Defined as ≥1 consecutive day of peritoneal dialysis after transition and censored at time of death, kidney transplantation, transfer home hemodialysis or administrative end of follow-up December 31st, 2018)
From first day after transfer to HD up to 180-day post transfer. Also measured at 90- and 365-day post transfer.
Transfer to Home Hemodialysis
Time Frame: From first day after transfer to HD until 180-day post transfer. Also measured at 90- and 365-day post transfer
Defined as ≥30 consecutive days of home hemodialysis censored at time of death, kidney transplantation, return to PD or administrative end of follow-up December 31st, 2018)
From first day after transfer to HD until 180-day post transfer. Also measured at 90- and 365-day post transfer

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2005

Primary Completion (Actual)

December 31, 2019

Study Completion (Estimated)

December 1, 2027

Study Registration Dates

First Submitted

February 20, 2026

First Submitted That Met QC Criteria

March 13, 2026

First Posted (Actual)

March 17, 2026

Study Record Updates

Last Update Posted (Actual)

March 17, 2026

Last Update Submitted That Met QC Criteria

March 13, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 2021-2531
  • 203760_1 (Other Grant/Funding Number: CIHR)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Based on restriction from the Canadian Institute for Health Information and our third party agreement

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Hemodialysis

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