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临床试验/NCT06677437
NCT06677437招募中不适用

Endovascular Preparation for Kidney Tranplantation

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2024年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
58
试验地点
1
主要终点
Evaluate the success of endovascular arterial preparation for grafting Renal.

研究概览

简要总结

This national study is a feasibility study. It wants to validate all stages of the endovascular preparation of the iliac axis up to the kidney transplant for patients in whom the installation of a tailor-made endoprosthesis was necessary beforehand.

These patients are currently at a therapeutic impasse. This strategy of renal transplantation on an iliac artery endoprosthesis could ultimately give them access to the transplant with an improvement in quality of life and survival, for lower costs of care for the hospital and safety. less social than treatment by hemodialysis

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient from 18 to 85 years old (beyond 85 years old, guidance must remain exceptional)
  • Patients with chronic renal failure
  • Waiting for a kidney transplant
  • Who have a vascular contraindication to renal transplantation because of their anatomical constraints.

排除标准

  • 1-All criteria contraindicating kidney transplant other than for arterial anatomical problems: All criteria contraindicating kidney transplant other than for arterial anatomical problems:
  • A progressive cancer, which is not cured,
  • An uncontrolled infectious disease,
  • Severe cardiovascular or respiratory disease making general anesthesia impossible,
  • Unstabilized psychiatric disorders or illness,
  • Dementia proven to have progressed after specialist advice
  • Major obesity, with a body mass index greater than 50 kg/m2
  • Patient refusal
  • Patient under curatorship
  • Pregnant woman
  • Patients for whom it will not be possible to organize regular medical follow-up

结局指标

主要结局

Evaluate the success of endovascular arterial preparation for grafting Renal.

时间窗: "From enrollment to the end of treatment at 12 months

The success of arterial preparation for renal transplantation will be evaluated by: * Collect safety estimators, absence of serious complications (hemorrhage, acute/subacute ischemia of the lower limb, death, serious post-operative cardiorespiratory event, failure of renal function for non-dialysis patients) Validity at 1 month of an endovascular preparation for renal transplantation by tailor-made arterial stent by the success of the installation, the absence of endoleak and the good anteroposterior positioning of the stent * Effectiveness at 1 month of endovascular preparation for renal transplantation by tailor-made arterial stent by permeability confirmed by Doppler ultrasound

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 (1)

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