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Evaluation of the Integrated Home Dialysis Model

P

Princess Alexandra Hospital

Status

Completed

Conditions

Kidney Failure, Chronic

Treatments

Procedure: Home hemodialysis
Procedure: Peritoneal dialysis

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT02278159
ANZ41367

Details and patient eligibility

About

The purpose of this study is to evaluate which home dialysis modality pattern (home hemodialysis [HHD], peritoneal dialysis [PD] or a combination of both, e.g. PD and then HHD) allows for the longest home dialysis survival, as defined by the time dialysed in a home environment. The investigators hypothesize that patients transferred from one home modality to another will have a longer home dialysis survival compared to patients treated only with PD or HHD.

Enrollment

11,600 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with PD/HHD 90 days after RRT initiation between January 1, 2000 and December 31, 2012 reported in ANZDATA
  • ≥ 18 years

Exclusion criteria

  • Less than 90 days of dialysis
  • < 18 years
  • Patients transferred to Australia/New Zealand after initiation of dialysis in another country

Trial design

11,600 participants in 4 patient groups

Peritoneal dialysis only
Description:
Patient on PD modality 90 days after renal replacement therapy initiation and not transferred to HHD
Treatment:
Procedure: Peritoneal dialysis
Home hemodialysis only
Description:
Patient on HHD 90 days after renal replacement therapy initiation and not transferred to PD
Treatment:
Procedure: Home hemodialysis
PD and HHD
Description:
Patient on PD 90 days after RRT initiation and transferred to HHD less than 90 days after PD failure
Treatment:
Procedure: Home hemodialysis
Procedure: Peritoneal dialysis
HHD and PD
Description:
Patient on HHD after RRT initiation and transferred to PD less than 90 days after HHD failure
Treatment:
Procedure: Home hemodialysis
Procedure: Peritoneal dialysis

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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