Clinical evaluation of postdilution on-line hemodiafiltration with reduced dialysate volume

Clinical evaluation of postdilution on-line hemodiafiltration with reduced dialysate volume - Clinical evaluation of postdilution on-line hemodiafiltration with reduced dialysate volume

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000057704

Enrollment

Registered

2025-04-26

Start date

2025-05-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with end-stage renal failure undergoing postdilution online hemodiafiltration

Interventions

Changes in dialysis fluid volume and treatment mode

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients undergoing post-dilution hemodiafiltration

Exclusion criteria

Exclusion criteria: 1. Patients who cannot provide written informed consent 2. Patients who are deemed inappropriate by the principal investigator

Design outcomes

Primary

Measure	Time frame
Amino acid and albumin leakage	—

Secondary

Measure	Time frame
Urea, creatinine, phosphorus, potassium, alfa1-microglobulin removal rate and removal amount, blood gas analysis, post-treatment fatigue, dialysis recovery time	—

Countries

Japan

Contacts

Public ContactHiroyuki Michiwaki

Kawashima Hospital Department of Clinical Engineering

michiwaki@khg.or.jp088-631-0110

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026