Viewing Study NCT03293134


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Study NCT ID: NCT03293134
Status: COMPLETED
Last Update Posted: 2017-09-26
First Post: 2017-05-02
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Clinical and Molecular Characterization of Cerebral Proliferative Vasculopathy
Sponsor: Assistance Publique - Hôpitaux de Paris
Organization:

Study Overview

Official Title: Clinical and Molecular Characterization of Cerebral Proliferative Vasculopathy
Status: COMPLETED
Status Verified Date: 2017-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: VPCA
Brief Summary: As principal objective, the study aims to:

1. Describe the spectrum and evaluate the frequency of angiodysplasia of the nevrax;
2. Establish the physiopathological basis of Fowler's syndrome;
3. Identify FLVCR2 partners and the signaling pathways involved;
4. Test new candidate genes: GPR124 and possible partners of FLVCR2.

As second objective, the study aims to:

* perform phenotype / genotype correlation if necessary;
* and propose a prenatal diagnosis in families with identified mutations.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: