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临床试验/NCT01774916
NCT01774916Unknown不适用

Identification of Genetic and Cellular Markers Associated With Vascular Endothelial Modifications in Cutaneous Arteriovenous Malformations

Assistance Publique Hopitaux De Marseille2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2013年1月最近更新:
适应症

试验速览

阶段
不适用
入组人数
50
试验地点
2
主要终点
The exploration of the microparticles, endothelial cells and progenitor cells

研究概览

简要总结

Cutaneous Arteriovenous malformations (AVM's) rare congenital high-flow vascular malformations in which arteries and veins are directly connected through a complex web of abnormal arteries and veins instead of a normal capillary network. Arterial feeders and enlarged draining veins directly connect through arteriovenous fistulas that create the "nidus". The natural history of AVMs is organized into a clinical staging system: during the first phase of quiescence, the arteriovenous malformation mimics a capillary malformation. After many years, the AVM may enlarge with loco-regional expansion and tissular destruction. At the ultimate stage, AVM may impact the heart function. They are considered non malignant but can expand and become a significant clinical risk when extensive. The management of these high flow AVM remains often problematic. Complete and large surgical excision of the nidus after hyperselective embolization is the only potential therapeutic solution but this, is often difficult if not impossible. There is no pathogenetic hypothesis for the development of these malformations. Histopathological examination (performed only on surgical resection specimen) is poor and does not provide sufficient evidence to assess the evolutivity or the severity of the MAV. Recent data hypothesize that these vascular malformations are associated with alterations of the vascular endothelium caused by genetic abnormalities involved in the control of angiogenesis and vascular homeostasis. The detection of these anomalies allows the search for cellular and genetic markers that might be useful to optimize the clinical classification, staging, predicting the evolution of these defects and some understanding of its pathophysiological mechanisms. To our knowledge, no studies to identify cellular markers / genetic and endothelial associated with the development of cutaneous AVMs have been published to date.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
盲法
None

入排标准

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

入选标准

  • Male or feminine Subject
  • Subject of 10 and more years old,
  • Subject weighing more than 55 kg. patients:
  • Subject presenting a cutaneous artério-venous deformation there outside of any other deformation or known vascular tumor.
  • Subject presenting no other susceptible pathology to influence endothéliaux markers (Renal insufficiency, inflammatory pathology chronicles, infections, pathologies cardiovascular, diabetes, evolutionary tumoral pathology).
  • volunteers:
  • Unhurt Subject of deformation or vascular tumor.
  • Subject presenting no other susceptible pathology to influence endothéliaux markers(scorers) (Renal insufficiency, inflammatory pathology chronicles, infections, pathologies cardiovascular).

排除标准

  • Subject of less than 10 years old
  • Subject weighing less than 55 kg
  • Subject presenting another type(chap) of vascular vascular deformation or tumor

结局指标

主要结局

The exploration of the microparticles, endothelial cells and progenitor cells

时间窗: 36 months

次要结局

  • investigate the relationship between endothelial markers and genetic and clinical characteristics of the disease(36 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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