Viewing Study NCT01907555



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Last Modification Date: 2024-10-26 @ 11:10 AM
Study NCT ID: NCT01907555
Status: COMPLETED
Last Update Posted: 2018-01-31
First Post: 2013-07-17

Brief Title: Clinical Molecular and Physiopathological Study of Cohen Syndrome and Cohen-like Syndromes
Sponsor: Centre Hospitalier Universitaire Dijon
Organization: Centre Hospitalier Universitaire Dijon

Study Overview

Official Title: None
Status: COMPLETED
Status Verified Date: 2018-01
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: None
Brief Summary: This project will make it possible to better understand the natural history of Cohen Syndrom and the phenotypes associated with mutations in the VPS13B gene to improve the therapeutic management of patients It will also provide a better description of Cohen-like syndrome for genetic counselling for the families concerned
Detailed Description: None

Study Oversight

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