Ignite Creation Date:
2024-05-05 @ 12:02 PM
Last Modification Date:
2024-10-26 @ 9:18 AM
Study NCT ID:
NCT00213811
Status:
COMPLETED
Last Update Posted:
2008-08-08
First Post:
2005-09-13
Brief Title:
Bardet-Biedl Syndrome Study Clinical and Genetic Epidemiology Study in Adults
Sponsor:
University Hospital Strasbourg France
Organization:
University Hospital Strasbourg France
Study Overview
Official Title:
Bardet-Biedl Syndrome Clinical and Genetic Epidemiology Study in the Adults
Status:
COMPLETED
Status Verified Date:
2008-08
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 study is based on the study of the natural history of a rare disorder the Bardet-Biedl syndrome BBS which is associated with retinitis pigmentosa polydactyly cognitive impairment obesity and kidney failure The clinical biological and radiological features of adult patients are studied In parallel a molecular study is performed on the known genes to date 8 genes from BBS1 to BBS8 and to identify new genes involved The parts of the study are combined in a phenotype-genotype correlation study
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