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临床试验/NCT03810911
NCT03810911终止2 期

Mechanisms of Erythropoietin Induced Hypertension

VA Office of Research and Development1 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2021年1月4日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
27
试验地点
1
主要终点
Within Group Change in Diastolic Blood Pressure in the Delayed Start Group

研究概览

简要总结

The investigators hypothesize that compared to untreated controls, erythropoietin (EPO) therapy in anemic patients with chronic kidney disease will raise diastolic blood pressure (BP). The magnitude of increase in diastolic BP at 12 weeks after treatment will be related to two factors. First, endothelial dysfunction and worsening of endothelial function from baseline to 4 weeks and second, the change of forearm blood flow in response to breathing oxygen and the change in this measure from baseline to 4 weeks. Study procedures include fasting blood draws, ambulatory blood pressure, urine collection, and forearm blood flow tests. The study hopes to accrue 160 subjects.

详细描述

Hypertension is a common but frequently overlooked and underreported adverse effect of erythropoietin (EPO) therapy. Recent trials have noted substantial cardiovascular risks associated with normalization of hemoglobin. The risk of strokes is strongly related to poorly controlled hypertension. Blood pressure was not measured the way it usually is in hypertension trials, so the investigators cannot be completely confident that the risk of strokes in this large randomized trial was not related to EPO-induced hypertension. New therapies, such as hypoxia-inducible factor (HIF) stabilizers are on the horizon but it remains to be seen whether these new drugs would have a lower or a higher risk for hypertension compared to EPO. Accordingly, understanding the mechanism of EPO-induced hypertension is urgent. The investigators hypothesize that compared to untreated controls, EPO therapy in anemic patients with chronic kidney disease (CKD) will raise diastolic blood pressure. The magnitude of increase in diastolic BP at 12 weeks after treatment will be related to endothelial dysfunction and worsening of endothelial function from baseline to 4 weeks. If the investigators understood the time course, the magnitude, and the mechanisms of EPO-induced hypertension (EIH) the investigators will better be able to design studies to compare the vascular effects of EPO and HIF stabilizers in the future. Thus, this study has the potential of improving the investigators' understanding of a common side effect of EPO by precisely quantifying the magnitude of BP change, its effects on endothelial function, and discovering the biomarkers of these adverse effects. Thus, the investigators can in the future robustly compare these effects of EPO with HIF stabilizers. This study is innovative because it will focus on the potential mechanisms by which EPO induces an increase in BP. The time-course and magnitude of change in BP will be assessed using the gold-standard measurement of 24 hour ambulatory BP recordings. The more frequent clinic BP recordings using validated methods will better allow us to track changes in BP over time. The investigators' lab is uniquely qualified to carry out these experiments due to a large experience with such types of studies. The investigators will examine endothelial function using a reference method -- that of flow-mediated dilatation -- which is established in the investigators' laboratory. The investigators will directly test the hypothesis whether endothelial function is responsible for the BP increase.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

盲法说明

The groups are randomized not the study drug. The groups will be known by both the participant and the investigator.

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

  • Stage 3 or 4 chronic kidney disease
  • Controlled hypertension with 24 hour ambulatory blood pressure monitoring less than 140/90 mmHg at baseline and treatment with at least 1 antihypertensive medication
  • Hemoglobin between 8 and 10 g/dL
  • No treatment with erythropoiesis-stimulating agents (ESA) within 3 previous months

排除标准

  • Need for packed red blood cells (RBC) transfusion in the previous 2 months
  • Myocardial infarction, stroke or hospitalization for heart failure in the past 2 months
  • In the assessment of the investigator, have hematologic, inflammatory, infectious, or other conditions that might interfere with the erythropoietic response

研究组 & 干预措施

Early start

Active Comparator

Participants given study drug immediately at randomization

干预措施: Darbepoetin (Drug)

结局指标

主要结局

Within Group Change in Diastolic Blood Pressure in the Delayed Start Group

时间窗: 12 to 24 weeks compared to baseline to 12 weeks

Within group change in diastolic blood pressure from 12 weeks to 24 weeks compared to change in diastolic blood pressure from baseline to 12 weeks in the delayed start group

Change in Diastolic Blood Pressure in EPO Treated Patients Compared to Delayed Start Controls

时间窗: Baseline to 12 weeks

In the delayed start group (the control group), the investigators will measure the change in diastolic blood pressure from 0 weeks to 12 weeks compared to the change in diastolic BP from 0 to 12 weeks in the immediate start group.

次要结局

  • Change in Systolic Blood Pressure in EPO Treated Patients Compared to Delayed Start Controls(Baseline to 12 weeks)
  • Number of Participants With Worsened Hypertension Status in Immediate Start Group Compared to Delayed Start Controls(Baseline to 12 weeks)
  • Number of Participants With Worsened Hypertension Status in Delayed Start Group Participants When They Were Not on EPO Compared to When They Were on EPO(baseline to 12 weeks vs 12 weeks to 24 weeks)
  • Change in Endothelial Function in Those Treated With EPO Compared to the Waitlisted Group(Baseline to 4 weeks)
  • Change in Urine Albumin to Urine Creatinine Ratio in the Delayed Start Group(Baseline to 16 weeks, baseline to 20 weeks, and baseline to 24 weeks)

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (1)

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