Incremental dialysis to improve health outcomes for kidney failure patients
The INCremental Dialysis to Improve Health Outcomes in People Starting Haemodialysis (INCH-HD) Study: a Randomised Controlled Trial
This study is testing if a new way of doing dialysis called incremental dialysis can help kidney failure patients feel better and improve their quality of life compared to the usual method.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 372 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | The University of Queensland Academic / other |
| Locations | 18 sites (Concord, New South Wales and 17 other locations) |
| Trial ID | NCT04932148 on ClinicalTrials.gov |
What this trial studies
The INCH-HD trial aims to evaluate whether incremental haemodialysis (HD) can preserve the quality of life for patients starting dialysis compared to conventional HD. This international, multicentre, prospective, adaptive, randomised, open-label trial will assess the non-inferiority of incremental HD in terms of quality of life outcomes measured at six months. The study addresses the high mortality and burden associated with traditional HD by exploring a potentially safer and more patient-friendly approach. Participants will be randomly assigned to either incremental or conventional HD to determine the best treatment strategy.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are beginning haemodialysis as their first treatment for kidney failure.
Not a fit: Patients with very low urine output or those unlikely to remain on haemodialysis for at least one year may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance the quality of life for patients with kidney failure while potentially reducing mortality rates.
How similar studies have performed: Observational studies suggest that incremental haemodialysis may offer advantages, but robust evidence for this approach is still lacking.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Adults (≥ 18 years of age) and 2. Commencing HD as their initial dialysis therapy and 3. Able to give informed consent Exclusion Criteria: 1. Urine output \<0.5Litres/day 2. Unlikely to be on HD for ≥1 year.
Where this trial is running
Concord, New South Wales and 17 other locations
- Concord Repatriation General Hospital — Concord, New South Wales, Australia (Recruiting)
- Northern Beaches Hospital — Frenchs Forest, New South Wales, Australia (Not_yet_recruiting)
- St George Hospital — Kogarah, New South Wales, Australia (Recruiting)
- Liverpool Hospital — Liverpool, New South Wales, Australia (Recruiting)
- John Hunter Hospital — New Lambton Heights, New South Wales, Australia (Recruiting)
- Port Macquarie Hospital — Port Macquarie, New South Wales, Australia (Recruiting)
- Royal North Shore Hospital — Saint Leonards, New South Wales, Australia (Not_yet_recruiting)
- Bundaberg Hospital — Bundaberg, Queensland, Australia (Recruiting)
- Cairns Hospital — Cairns, Queensland, Australia (Recruiting)
- Redland Hospital — Cleveland, Queensland, Australia (Not_yet_recruiting)
- Logan Hospital — Logan City, Queensland, Australia (Recruiting)
- Toowoomba Hospital — Toowoomba, Queensland, Australia (Recruiting)
- Princess Alexandra Hospital — Woolloongabba, Queensland, Australia (Recruiting)
- Royal Adelaide Hospital — Adelaide, South Australia, Australia (Recruiting)
- Monash Health — Melbourne, Victoria, Australia (Recruiting)
- Eastern Health — Melbourne, Victoria, Australia (Recruiting)
- Fiona Stanley Hospital — Murdoch, Washington, Australia (Not_yet_recruiting)
- University Health Network- University of Toronto — Toronto, Ontario, Canada (Not_yet_recruiting)
Study contacts
- Principal investigator: Peter Kerr, Prof — University of Queensland, Monash University
- Study coordinator: Lisan Mulvey
- Email: inch-hd.trial@uq.edu.au
- Phone: +61 417 690 237
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.