Evaluation of clinical characteristics (solute removal characteristics) by different dilution methods of hemodiafilter MFX-W eco series

Okada Kazuyoshi0 个研究点目标入组 8 人开始时间: 2023年3月24日最近更新: 2024年4月1日

适应症

试验速览

暂无简介。

•Patients who meet all of the following criteria are eligible for this study.
•(1)Patients who have undergone online HDF for more than 1 month at the time of informed consent
•(2)Patients who can maintain a stable blood flow rate of 280 mL/min
•(3)Patients using a hemodiafilter with a membrane area of 2.5m2 or more
•(4)Patients whose dialysis time is longer than 4 hours
•(5)Patients who are ambulatory
•(6)Patients who have given written informed consent to participate in this study
•(7)Men and women aged 18 or over and under 85 at the time of obtaining consent

•In consideration of the safety of the study subjects, patients who meet any of the following critria will be excluded from this study.
•(1) Patients who need to take other blood purification therapies such as peritoneal dialysis that may affect the evaluation of research equipment during the research period
•(2) Patients who have a history of acute symptoms such as anaphylactic reactions caused by polyethersulfone membranes or polyvinylpyrrolidone (PVP) in the past
•(3) Patients participating in other clinical studies that may affect the results of this study during the research period
•(4)Those with renal failure due to serious illness.
•(5) Other patients ineligible whom the principal investigator deems to conduct this study

发起方

Okada Kazuyoshi