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Performance comparison of hollow-fiber dialyzers, VPS-VA and VPS-HA

Performance comparison of hollow-fiber dialyzers, VPS-VA and VPS-HA - Clinical Study of VPS-VA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000030993
Enrollment
10
Registered
2018-01-31
Start date
2018-02-01
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

Chronic Kidney Disease (End Stage Renal Disease)

Interventions

Dialysis therapy using VPS-HA for a week. Hollow-fiber dialyzers will be changed from VPS-HA to VPS-VA. Dialysis therapy using VPS-VA for two weeks.

Sponsors

Toho Hospital, Sanshikai Medical Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients on stable maintenance dialysis therapy using VPS-HA at least three months. 2)Patients with capable of dialysis therapy using the type IIa hollow-fiber dialyzer. 3)Patients with capable of obtaining blood flow rate >= 200 mL/min. 4)Patients who are capable to participate in the study as outpatients. 5)Patients capable of understanding the informed consent form. 6)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 with a medical history of anaphylaxis symptoms caused by vitamin E-coated membrane. 4)Patients in the opinion of the principal investigator to disqualify from participation.

Design outcomes

Primary

MeasureTime frame
Beta 2-microglobulin clearance

Countries

Japan

Contacts

Public ContactMasaki Matsumura

Toho Hospital, Sanshikai Medical Corporation Kidney dialysis center

me6341mm@toho-hp.jp0277-76-6311

Outcome results

None listed

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