Genetic Analysis of Familial Brain Aneurysms
Linkage Analysis of Familial Intracranial Aneurysms
2 other identifiers
observational
300
1 country
1
Brief Summary
This study will investigate cerebral (brain) aneurysms and their possible inheritance patterns in families. It will try to determine how often brain aneurysms occur in families in which more than one member has had an aneurysm and to find the gene or genes that contribute to their development. People in families in which more than one family member had a cerebral aneurysm are eligible for this 1-day study. They will undergo the following procedures:
- Blood will be drawn (no more than 3 to 4 tablespoons) for research to identify genes that contribute to the development of brain aneurysms.
- A magnetic resonance angiograph (MRA) scan will be done to examine a specific brain area where aneurysms typically occur. Magnetic resonance imaging uses a strong magnetic field and radio waves to produce images of the brain and detect abnormalities. If a more detailed picture of the brain is needed than can be obtained with MRA, a more specific MRA scan will be done using a contrast dye to enhance the images. Patients may be invited to participate in related NIH research studies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2001
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2001
CompletedFirst Submitted
Initial submission to the registry
March 1, 2001
CompletedFirst Posted
Study publicly available on registry
March 2, 2001
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2002
CompletedMarch 4, 2008
March 1, 2002
March 1, 2001
March 3, 2008
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Participants and their relatives that are affected or at a higher risk for cerebral aneurysms will be enrolled in this protocol.
You may not qualify if:
- For the MR Angiograph portion of the study, any participant that is not able to sign the Clinical Center consent form due to metal implants, pregnancy, claustrophobia, or an allergy to gadolinium as a contrast will be excluded from the imaging part of the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Human Genome Research Institute (NHGRI)
Bethesda, Maryland, 20892, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Sponsor Type
- NIH
Study Record Dates
First Submitted
March 1, 2001
First Posted
March 2, 2001
Study Start
February 1, 2001
Study Completion
March 1, 2002
Last Updated
March 4, 2008
Record last verified: 2002-03