Genome-wide Analysis of Single Nucleotide Polymorphisms of Brain Arteriovenous Malformations and Cerebral Aneurysm
|ClinicalTrials.gov Identifier: NCT01801488|
Recruitment Status : Terminated (Low enrollment)
First Posted : February 28, 2013
Last Update Posted : November 25, 2015
|Condition or disease|
|Arteriovenous Malformations Intracranial Aneurysm Subarachnoid Hemorrhage|
|Study Type :||Observational|
|Actual Enrollment :||5 participants|
|Observational Model:||Case Control|
|Official Title:||Genome-wide Analysis of Single Nucleotide Polymorphisms of Brain Arteriovenous Malformations and Cerebral Aneurysm|
|Study Start Date :||November 2011|
|Primary Completion Date :||March 2014|
Patients receiving surgical intervention for an intracranial arterial-venous malformation.
Patients receiving surgical intervention for a ruptured intracranial aneurysm.
Patients receiving surgical intervention for an unruptured intracranial aneurysm.
- Risk gene expression [ Time Frame: Within one week of sample collection. ]The samples will be frozen after collection and then analyzed.
Biospecimen Retention: Samples With DNA
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01801488
|United States, New York|
|SUNY Upstate Medical University|
|Syracuse, New York, United States, 13210|
|Principal Investigator:||Eric M Deshaies, MD||SUNY Upstate Medical University Neurosurgery|