- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07477210
Examine the Epidemiology and Outcomes of Transitions From PD-to-HD in Canada (UPLIFT-PD CORR)
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
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Quebec
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Montreal, Quebec, Canada, H1T 2M4
- CIUSSS de l'Est-de-l'ile de Montréal
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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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.
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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.
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From PD initiation until 1-year after PD start Also assessed at from PD initation until 2- and 5-year after PD start.
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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
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Censored for kidney transplantation, transfer home hemodialysis, return to PD or administrative end of follow-up December 31st, 2018
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From first day after transfer up to 1-year post transfert. Also assessed ad 2- and 5-year post transfer
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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.
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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)
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From first day after transfer to HD up to 180-day post transfer. Also measured at 90- and 365-day post transfer.
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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
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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)
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From first day after transfer to HD until 180-day post transfer. Also measured at 90- and 365-day post transfer
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
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)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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