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NCT Number: NCT06642597

STarting incrEmental Prescription of Peritoneal Dialysis

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Blacktown, New South Wales, Australia

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About this study

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

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Incremental PD

Other

Incremental PD: Commence PD using goal-directed PD prescription ≤14 exchanges/week for continuous ambulatory PD (CAPD) or ≤21 exchanges/week for automated PD (APD) with no day dwell until an indication for increase in the PD dose (trigger point) is reached.

Full dose PD

Other

Full dose PD: Commence with 24 hours, 7 days/week PD (i.e., CAPD ≥28 exchanges/week or APD (overnight) with day dwell (i.e., no dry abdomen)).

Primary outcomes

  1. Quality of Life (QoL)

    Time frame: From enrollment to the end of treatment at 6 months

    Symptom burden-related QOL 6 months after dialysis start, assessed by the Symptoms and Problems of Kidney Disease (SPKD) component of KDQOL-36 (0 to 100; worst to best).

Secondary outcomes

  1. Residual Kidney Function (RKF)

    Time frame: From enrollment to 3, 6, 9, 12 and 18 months

    Slope of RKF decline over time modelled with linear regression of the arithmetic means of 24-hour urinary urea and creatinine clearances at months 3, 6, 9, 12 and 18

  2. Anuria

    Time frame: From enrollment to 3, 6, 9, 12 and 18 months

    Proportion of patients with anuria (<100mL/24h) at months 3, 6, 9, 12 and 18

  3. Serious adverse event

    Time frame: Enrollment to 18 months

    Number of category type of serious adverse events

  4. Death

    Time frame: Enrollment to 18 months

    Time to all-cause mortality

  5. Major cardiovascular event

    Time frame: Enrollment to 18 months

    Time to first major cardiovascular event (defined as acute myocardial infarction)

  6. Peritonitis

    Time frame: Enrollment to 18 months

    Time to first peritonitis event

  7. Non-elective hospitalisations

    Time frame: Enrollment to 18 months

    Number of non-elective hospital admissions

  8. Hospitalisations

    Time frame: Enrollment to 18 months

    Hospitalisation for fluid overload, hyperkalaemia, or uraemic complications; episodes of hyperkalaemia (≥6mmol/L)

  9. Quality of Life (QOL) and life participation

    Time frame: Enrollment to 18 months

    QOL and life participation: quarterly KDQOL-36 (physical and mental composite scores; effects and burden of kidney disease) and the SF6D (a component of the KDQOL)

Study contacts

Contact information is provided by the study sponsor or research team.

Laura Hickey

CONTACT

[email protected]

+61 427 911 414

Professor Yeoungjee Cho

CONTACT

[email protected]

+61 7 3176 5080

Sponsors and collaborators

Lead sponsor

The University of Queensland

Other

Registry information

Official study title

An International, Multi-centre, Randomised Controlled Trial Co-designed With Consumers With Lived Experience of Peritoneal Dialysis (PD) to Determine the Optimal Approach to Starting Patients With Kidney Failure on PD

Acronym: STEP-PD

Important dates

Study start
2025
Primary completion
2029
Study completion
2029
First posted
Oct 15, 2024
Registry last updated
Jun 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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