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临床试验/NCT05936021
NCT05936021进行中(未招募)不适用

Clinical Validation Study for Optimization of Anemia MAnagement in Hemodialysis Patients With End Stage Kidney Disease Using the Dialysis Anemia TReatmenT Model

Intermountain Health Care, Inc.4 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2023年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
80
试验地点
4
主要终点
Time hemoglobin levels are maintained within acceptable range

研究概览

简要总结

This is a human subject research study conducted in patients undergoing dialysis treatment with darbepoetin alfa at Intermountain Utah Dialysis and Intermountain Medical Center Dialysis Services. The purpose is to test a dose recommendation algorithm that may reduce hemoglobin variability and drug cost.

详细描述

Hemoglobin cycling is an outcome of treating long-term dialysis patients for anemia using erythropoiesis-stimulating agents (ESAs), and represents a conundrum for practitioners. While patients with low hemoglobin levels suffer from anemia, high hemoglobin levels may lead to blood clots and subsequent health risks. The current protocol for ESA dosing often results in suboptimal dosing that leads to hemoglobin cycling, which can have a negative impact on patient survival. To this end, we have developed a personalized method for ESA dosing that controls anemia in dialysis patients that is similar to the commercial product sold by PhySoft. Our method, the Dialysis Anemia Treatment Model, uses a mathematical model for erythropoiesis that takes each patient's physiology into account, predicting the optimal dose of ESA for that patient to prevent hemoglobin cycling. The goal of this computer-aided approach is to reduce hemoglobin cycling and the amount of drug used by predicting optimal doses to keep the patient's hemoglobin within the desired range. This is a human subject research study to validate the model in the clinic and demonstrate that it is able to minimize hemoglobin cycling in patients and reduce the amount of ESA drug administered.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Supportive Care
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

  • Males and females (≥ 18 years of age) with End Stage Kidney Disease undergoing in-center hemodialysis
  • 150 days of hemoglobin readings and Aranesp doses without a hospitalization relevant to the condition of anemia

排除标准

  • Inflammation as characterized by ferritin levels greater than 1000 ng/mL
  • Patients with active cancer
  • Patients with PTH greater than 1,000 pg/mL
  • Active GI Bleed
  • Hospitalization relevant to ESRD in last 150 days or during study
  • Patients receiving Procrit rather than Aranesp.

结局指标

主要结局

Time hemoglobin levels are maintained within acceptable range

时间窗: 90 days after the intervention

Time hemoglobin levels are maintained within acceptable range

Reduction of hemoglobin cycling in dialysis patients

时间窗: 90 days after the intervention

Reduction of hemoglobin cycling

次要结局

  • Reduction in quantity of drug administered to patients(90 days after the intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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