跳至主要内容
临床试验/NCT03382301
NCT03382301已完成2 期

Impact of a Ciclosporin A Preconditioning for Prevention of Ischemia-reperfusion Injury After Renal Artery Stenosis Dilation

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2018年8月28日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
5
试验地点
1
主要终点
Difference in relative increase (baseline and 3 months after) of global renal perfusion between the two groups

研究概览

简要总结

Renal artery stenosis is one the leading cause of secondary hypertension. Previous randomized controlled trials in humans have failed to demonstrate an improvement of renal function after stenosis dilation, probably because of a selection bias with more severe patients being excluded from randomization. Renal ischemia-reperfusion injuries have also not been taken into account. Indeed, reperfusion leads to a rapid renal blood flow recovery associated with renal ischemia-reperfusion injuries.

Mitochondrial permeability transition pore (mPTP) is a key player in the occurrence of ischemia reperfusion injuries because its opening leads to mitochondria leakage and cell death. However, preconditioning whether pharmacological or ischemic can prevent mPTP opening and protect cells. Ciclosporin A can prolong mPTP closing during reperfusion and reduce renal and cardiac tissular lesions. Another mPTP blocker (Bendavia) has been associated with an improvement of renal blood flow (RBF) and glomerular filtration rate (GFR) after renal artery stenosis dilation at 6 weeks in pigs. Based on a recent study, dilation overall benefit could be secondary to an improvement of the contralateral kidney GFR and tissue oxygen content, requiring a single kidney evaluation of those renal functional parameters. The investigators previously demonstrated that dose and timing of ciclosporin A preconditioning is key to protect kidneys from ischemia-reperfusion injuries. Previous controlled trials that failed to demonstrate a benefit of ciclosporin A conditioning have used post conditioning on necrotic cells. Considering kidney ischemia-reperfusion injuries, preconditioning have led to more encouraging results compared to ciclosporin A post conditioning in animals. Therefore the investigators aim to conduct the first clinical study of ciclosporin A preconditioning for prevention of kidney ischemia-reperfusion injuries after renal artery stenosis dilation.

Using renal functional imaging and the new PET-MRI (Positron Emission Tomography-Magnetic Resonance Imaging) combined device, the investigators will evaluate kidney perfusion, oxidative metabolism, glomerular filtration rate and oxygen content before and 3 months after renal artery stenosis dilation with or without a ciclosporin A preconditioning.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • Patients over 50 years of age
  • For women : only menopausal women
  • Estimated Glomerular filtration rate ≥ 25 mL/min/1.73m2
  • Renal artery stenosis with ≥ 70 % caliber reduction (Doppler or scanner or MRI)
  • No controlateral stenosis
  • Kidney size ≥ 7 cm
  • Only atheromatous renal artery stenosis
  • Resistant hypertension and/or rapid loss of kidney function and/or flash pulmonary edema
  • Collective decision of dilation after a multidisciplinary meeting

排除标准

  • Inclusion in another study
  • Protected adults
  • Person without a social security coverage
  • Imprisoned person
  • Systolic blood pressure >180 mmHg and/or diastolic blood pressure > 110 mmHg
  • Non atheromatous renal artery stenosis
  • Single kidney
  • Multiple myeloma
  • Iodine contrast agents allergy
  • Ciclosporin A hypersensibility
  • Severe other medical conditions that could be exacerbated by Iodine injection (cancer, lymphoma, active Hepatitis B, active Hepatitis C, uncontrolled HIV)
  • Previous radiation exposure (above 20 mSv (millisievert) in the last 6 months before inclusion)
  • MRI contra indications (MRI incompatible pacemaker or insulin pomp, metal clip, MRI incompatible cardiac valve, dental brace, claustrophobia)

研究组 & 干预措施

Ciclosporin A preconditioning

Experimental

Ciclosporin A preconditioning before renal artery stenosis dilation

干预措施: Ciclosporin A preconditioning before renal artery stenosis dilation (Drug)

NaCl preconditioning

Placebo Comparator

干预措施: NaCl preconditioning before renal artery stenosis dilation (Drug)

结局指标

主要结局

Difference in relative increase (baseline and 3 months after) of global renal perfusion between the two groups

时间窗: 3 months after renal artery stenosis dilation

Global renal perfusion is assessed by 15O labeled water PET (Positron Emission Tomography) imaging

次要结局

  • Difference in the relative increase (baseline and 3 months after) of global renal oxidative metabolism between the two groups(3 months after renal artery stenosis dilation)
  • Difference in the relative increase (baseline and 3 months after) of global renal oxygen content between the two groups(3 months after renal artery stenosis dilation)
  • Difference in the relative increase (baseline and 3 months after) of global glomerular filtration rate between the two groups(3 months after renal artery stenosis dilation)
  • Difference in the relative increase (baseline and 3 months after) of single-kidney perfusion (ischemic versus contralateral kidney) between the two groups(3 months after renal artery stenosis dilation)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验