Viewing Study NCT02585739



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Last Modification Date: 2024-10-26 @ 11:51 AM
Study NCT ID: NCT02585739
Status: COMPLETED
Last Update Posted: 2015-10-23
First Post: 2015-10-22

Brief Title: Cluster Headache and SPINK-1 Gene
Sponsor: Assistance Publique Hopitaux De Marseille
Organization: Assistance Publique Hopitaux De Marseille

Study Overview

Official Title: Cluster Headache and SPINK-1 Gene
Status: COMPLETED
Status Verified Date: 2015-10
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: Cluster headache CH is a rare excruciating primary headache disorder A genetic basis has been suggested by family and twin studies but the mode of transmission seems to vary and the amount of heritability is unclear

The number of genetic association studies investigating variants implicated in the pathophysiology of CH is limited The HCRTR2 1246G A and the ADH4 925A G polymorphisms have been associated with CH The former has been confirmed and may affect the hypothalamic hypocretin system The aim of the present study was to investigate the possible link between SPINK 1 gene and cluster headache
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
Secondary IDs
Secondary ID Type Domain Link
RC12_3011 OTHER APHM None