Skip to content

Performance evaluation of ABH-PA

Effectiveness(performance) evaluation trial of hemodiafilter ABH-PA at pre-dilution and post-dilution on-line hemodiafiltration

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs062190020
Enrollment
8
Registered
2019-10-15
Start date
2020-01-13
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

Chronic Kidney Disease Chronic Kidney Disease

Interventions

On-line hemodiafiltration therapy using ABH-22PA for six weeks.
Hemodiafiltration

Sponsors

OKADA Kazuyoshi
Lead Sponsor
ASAHI KASEI MEDICAL CO., LTD
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients on stable maintenance on-line hemodiafiltration therapy at least one month. 2) Patients with capable of obtaining blood flow rate >= 280 mL/min. 3) Patients who are undergoing hemodiafiltration with a hemodiafiler of membrane area >= 2.2m^2. 4) Patients who are undergoing hemodiafiltration for >= 4 hours per treatment. 5) Patients who are capable to participate in the study as outpatients. 6) Patients capable of understanding the informed consent form. 7) Patients >= 20 years and <85 years of age at the time of informed consent.

Exclusion criteria

Exclusion criteria: 1)Patients requiring another blood purification therapy such as peritoneal dialysis other than hemodiafiltration within this study period. 2)Patients with a medical history of anaphylaxis symptoms caused by polysulfone or polyvinylpyrrolidone (PVP). 3)Patients who will participate in other clinical trials that may influence the results of this study within this study period. 4)Patients in the opinion of the principal investigator to disqualify from participation.

Design outcomes

Primary

MeasureTime frame
Reduction rate, Removal amount, Clear space, Albumin leakage, Transmembrane pressure, Antithrombotic property

Secondary

MeasureTime frame
Inflammatory response

Contacts

Public ContactHiroyuki MICHIWAKI

Kawashima Touseki clinic

michiwaki@khg.or.jp+81-88-634-0200

Outcome results

None listed

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