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Clinical effects of polysulfone membrane, NV-13U

Clinical effects of polysulfone membrane, NV-13U - Clinical effects of polysulfone membrane, NV-13U

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011764
Enrollment
12
Registered
2013-09-17
Start date
2011-11-21
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

end-stage renal failure

Interventions

four weeks of APS-13SA use, amd for two weeks of the washout period, and then four weeks of NV-13U use four weeks of NV-13U use, and for two weeks of the washout period, and then four weeks of APS-13

Sponsors

National Defense Medical College
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: end-stage renal failure patients with stable outpatient maintenance hemodialysis 60 years or older

Exclusion criteria

Exclusion criteria: hemodialysis patients without any cancer or acute Inflammation

Design outcomes

Primary

MeasureTime frame
We use conventional polysulfone film (APS - 13SA) and new polysulfone film (NV- 13 U) in 4-week crossover for a hemodialysis patients twice. And we measure solute removal ability (clearance, quantity of removal, removal rate), antithrombotic (activated solidification time, solidification ability) and compare them.

Secondary

MeasureTime frame
We measure a very small amount of albumin in the biocompatible (leukocyte image) dialysis waste fluid of the polysulfone film (APS - 13SA) and new polysulfone film (NV- 13 U) and compare the safety for the elderly patient.

Countries

Japan

Contacts

Public ContactKaori Ishizeki

National Defense Medical College Hospital Department of Blood Purification

halfmoon@ndmc.ac.jp04-2995-1511

Outcome results

None listed

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