Skip to main content
Clinical Trials/NCT01774916
NCT01774916
Unknown
Not Applicable

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

Assistance Publique Hopitaux De Marseille1 site in 1 country50 target enrollmentJanuary 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cutaneous Arteriovenous Malformations
Sponsor
Assistance Publique Hopitaux De Marseille
Enrollment
50
Locations
1
Primary Endpoint
The exploration of the microparticles, endothelial cells and progenitor cells
Last Updated
11 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
July 2016
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 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).

Exclusion Criteria

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

Outcomes

Primary Outcomes

The exploration of the microparticles, endothelial cells and progenitor cells

Time Frame: 36 months

Secondary Outcomes

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

Study Sites (1)

Loading locations...

Similar Trials