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临床试验/NL-OMON41932
NL-OMON41932已完成不适用

Effects of Lumbar Sympathetic Blockade Renal Plasma Flow and Glomerular Filtration Rate. - RELIEF study

Academisch Medisch Centrum0 个研究点目标入组 3 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
3

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - age *18 years
  • - able to give informed consent
  • - no recent changes or expected changes in antihypertensive medications or psychopharmaca
  • - we aim at including at least 50% of the patients with an eGFR < 60ml/min. If the number of patients with eGFRs <60ml/min who are willing to participate in the study is more than patients with eGFR> 60ml/min: the patients with the lowest eGFRs will be selected for inclusion.

排除标准

  • - not willing to be informed about unexpected findings during the study
  • - neurologic disease
  • - Lung disease
  • - pregnancy
  • - renal replacement therapy (hemo- or peritoneal dialysis)
  • - iodine allergy
  • - allergy for shellfish
  • - not being able to resign from cigarette smoking/ nicotine use in any form, for >20 hours ;PLEASE NOTE: the second GFR and RPF measurements will only be performed in patients with a successful persistent blockade that has been clinically assessed by the pain specialist. In the case of LSB: treatment is regarded as successful upon vasodilatation and in the case of splanchnic blockade relief of pain.

研究者

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