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Development of a new method to control albumin leakage during on-line hemodiafiltration (HDF) therapies for maintenance dialysis patients (New Qs control program of JMS GC-X01 dialysis machine using hemodiafilter ABH-22PA)

Development of a new method to control albumin leakage during on-line hemodiafiltration (HDF) therapies for maintenance dialysis patients (New Qs control program of JMS GC-X01 dialysis machine using hemodiafilter ABH-22PA) - Clinical research to develop the new Qs control program

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000029203
Enrollment
5
Registered
2017-09-20
Start date
2017-09-20
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 Failure (End Stage Renal Disease)

Interventions

Hemodiafiltration therapy using JMS GC-X01 dialysis machine and hemodiafilter ABH-22PA for 8 weeks.

Sponsors

Kaikoukai Medical Foundation Meiko Kyoritsu Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients on stable maintenance hemodialysis therapy at least one month on a 3 times per a week schedule with not less than 4 hours per a treatment. 2)Patients corresponding to the following at the time of registration - Total protein: 5.0 - 7.0 g/dL - Hematocrit: 28 - 38%. 3)Patients with capable of obtaining blood flow rate >250 mL/min. 4)Patients who are capable to participate in the study as outpatients. 5)Patients capable of understanding the informed consent form. 6)Aged 20 to <80 years 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 hypoalbuminemia. 4)Female patients who are or have possibility of pregnant, or breast feeding. 5)Patients who have a history of liver, heart, or lung diseases (ex. Decompensated cirrhosis). 6)Patients with previously untreated malignant tumors. 7)Patients with dementia. 8)Patients having a plan of participating in any other clinical trial within this study period. 9)Patients in the opinion of the principal investigator to disqualify from participation.

Design outcomes

Primary

MeasureTime frame
Amount of albumin leakage

Countries

Japan

Contacts

Public ContactMasahiro Taoka

Kaikoukai Medical Foundation Meiko Kyoritsu Clinic

m-taoka@kaikou.or.jp052-698-3077

Outcome results

None listed

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