Viewing Study NCT03293134



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Last Modification Date: 2024-10-26 @ 12:32 PM
Study NCT ID: NCT03293134
Status: COMPLETED
Last Update Posted: 2017-09-26
First Post: 2017-05-02

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

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 Fowlers 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: None
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?: None