JPRN-jRCTs062190020Completed未知
Effectiveness(performance) evaluation trial of hemodiafilter ABH-PA at pre-dilution and post-dilution on-line hemodiafiltration
OKADA Kazuyoshi0 sites8 target enrollmentStarted: October 15, 2019Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 8
Study Overview
Brief Summary
It was confirmed that hemodiafilter ABH-PA changed its removal performance depending on the amount of replacement fluid in both pre-dilution and post-dilution in HDF mode. Further, it was confirmed that the removal performance of ABH-PA tends to increase as the amount of replacement liquid increases. In addition, no significant difference was observed in the inflammatory maker level between the pre-dilution and the post-dilution.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- >= 20age old to < 85age old (—)
- Sex
- All
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
- •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.
Investigators
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