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Recruiting Not applicable NCT06642597

STarting incrEmental Prescription of Peritoneal Dialysis

No applicable phase (e.g. observational)
Conditions: Peritoneal Dialysis (PD) Kidney Failure

Sponsor: The University of Queensland

trial.available_in: БГ
Overview
Kidney failure is fatal without dialysis. Peritoneal dialysis (PD) completed at home offers greater flexibility and autonomy for patients . However, PD is often prescribed for 24 hours/day, 7 days/week for every patient starting dialysis. This practice is not evidence-informed, may be unnecessary and potentially harmful. The STEP-PD trial aims to determine the optimal approach to commencing patients on PD through starting at low dose PD and incrementing over time.
Description
The STEP-PD study is an investigator-initiated, pragmatic, international, multicentre, prospective, adaptive, randomised, open-label, parallel group, non-inferiority trial led by an international multi-disciplinary team of clinician scientists, nephrologists, consumers, social scientists, trialists, health economists, dialysis nurses, statisticians, and registry experts. The STEP-PD trial is co-designed with consumers with lived experience of peritoneal dialysis (PD) to determine the optimal approach to starting patients with kidney failure on PD. Specifically, this trial will test the hypothesis that, compared with full dose PD, starting patients on incremental start PD preserves symptom burden related quality of life (QOL), reduces dialysis burden, is safe, is more environmentally sustainable and costs less for patients, the community and the healthcare system. The STEP-PD trial has the potential to transform and personalise the treatment of kidney failure globally by providing definitive evidence on the patient-prioritised question regarding the effectiveness and safety of incremental start PD, particularly in relation to the patient-critical outcome of symptom burden-related QOL. Favourable results would lead to a paradigm shift in how patients are started on PD, thereby mitigating unnecessarily burdensome, expensive, and possibly harmful treatment.
Who can participate
Inclusion Criteria: * adults (≥18 years) commencing PD as their first dialysis therapy (and been on dialysis for \<1 month) * able to give informed consent Exclusion Criteria: * urine output \<0.5L/day * previous kidney transplant * unlikely to be on dialysis for ≥1 year. * known or planned pregnancy during the trial
Locations 4
Australia (1)
Blacktown
Blacktown , New South Wales
Katrina Chau, Associate Professor
South Korea (1)
Hallym University Sacred Heart Hospital
Chuncheon , Gangwon-do
Jwa-Kyung Kim, Professor
Taiwan (1)
Taichung Veterans General Hospital
Taichung , Xitun District
Mu Chi Chung, Associate Professor
Thailand (1)
King Chulalongkorn Memorial Hospital
Bangkok , Pathum Wan
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
19.09.2025
Completion date
30.09.2029
Registry ID
NCT06642597
Source
anzctr
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