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临床试验/NCT04020757
NCT04020757终止2 期

H+ Mobilization With Dialysate Bicarbonate Variation

Tufts Medical Center2 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2019年6月12日最近更新:
适应症

试验速览

阶段
2 期
状态
终止
入组人数
13
试验地点
2
主要终点
Lactate levels

研究概览

简要总结

The aims of the proposed studies are first to delineate the physiological response of End Stage Kidney Disease (ESKD) patients to exposure to a bath [HCO3-] of 35 mEq/L and an [acetate] of 4 mEq/L, and second, to determine whether reducing bath [HCO3-] will have the expected effect of decreasing or abolishing stimulation of organic acid production. A secondary endpoint will be whether the patients tolerate such a reduction and its impact on pre-dialysis blood [HCO3-]. If the outcome is positive in both regards, future studies will measure well-being and outcomes with reduced bath [HCO3-].

研究设计

研究类型
Interventional
干预模型
Sequential
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

  • Patients must be 18 years or older,
  • Have been on dialysis for at least 1 year,
  • Be stable on treatment (i.e., without frequent changes in their dialysis prescription, or recent hospitalizations),
  • Be reasonably nourished (serum albumin > 3.5 g/dl and not currently receiving oral nutritional supplement through DCI).
  • Self-reported urine output of <200 cc/day
  • Functioning arteriovenous fistulas or grafts for dialysis access
  • Currently dialyzing at a dialysate [HCO3-] of 33-37 mEq/L.

排除标准

  • Acute illnesses of any kind,
  • Hospitalization in the prior 3 months (except for vascular access related),
  • Significant congestive heart failure, liver or lung failure.
  • Pre-dialysis blood [HCO3-] <19 mEq/L) (to reduce the risk of metabolic acidosis )

结局指标

主要结局

Lactate levels

时间窗: through study completion, a period of 3 weeks

7 tests conducted through the dialysis treatment after the long interdialytic interval

H+ mobilization

时间窗: through study completion, a period of 3 weeks

7 tests conducted through the dialysis treatment after the long interdialytic interval

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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