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临床试验/NCT06574425
NCT06574425Enrolling By Invitation4 期

A Multicenter, Prospective, Cohort Study on the Safety and Efficacy of Long-term, High Blood Flow Hemoadsorption Therapy in Patients Undergoing Maintenance Hemodialysis

Dongliang Zhang, MD1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年8月28日最近更新:
适应症

试验速览

阶段
4 期
状态
Enrolling By Invitation
发起方
入组人数
80
试验地点
1
主要终点
protein-bound toxins

研究概览

简要总结

Objective:The purpose of the study is to confirm that extending the duration of hemoadsorption (HA) and increasing blood flow during the HA+hemodialysis (HD) treatment process is safe and feasible, and to verify that extending the HP treatment duration can further increase the clearance of protein-bound uremic toxins.

Methods: The study employs a multicenter, prospective, cohort design with a self-controlled before-and-after comparison. The duration of HA+HD treatment for maintenance hemodialysis (MHD) patients is extended to 4 hours, and the extracorporeal blood flow rate is increased to over 250-350 ml/min. The safety of the treatment is assessed by evaluating the safety of the procedure; the levels of relevant toxins in the patients' blood are measured before and after treatment, and the clearance rate of uremic toxins after a single treatment is calculated and compared with the self-controlled before-and-after data to determine whether the modified protocol can remove more uremic toxins.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Maintenance Hemodialysis Patients with Uremia receive regular HA+HD treatment

排除标准

  • Plasma albumin <30g/L, severe malnutrition or cachectic state; platelet count <40×10^9/L or >300×10^9/L; hypercoagulable state allergy to the hemoperfusion device; new cardiovascular or cerebrovascular diseases; poor vascular access function, extracorporeal circulation blood flow unable to reach 250ml/min ultrafiltration volume >4500ml in a single dialysis session use of non-heparin anticoagulants inability to comply with the procedures of this study other conditions deemed unsuitable for participation in this study by the investigator

结局指标

主要结局

protein-bound toxins

时间窗: 1month

the clearance of protein-bound toxins will change

次要结局

未报告次要终点

研究者

发起方
Dongliang Zhang, MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dongliang Zhang, MD

Director of Nephrology Department of Beijing Jishuitan Hospital

Capital Medical University

研究点 (1)

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