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Clinical Trials/NCT01060800
NCT01060800
Completed
Not Applicable

The Genetics of Chiari Type I Malformation (CMI) With or Without Syringomyelia

Duke University1 site in 1 country2,000 target enrollmentStarted: June 2009Last updated:
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ConditionsChiari Type I Malformation

Overview

Phase
Not Applicable
Status
Completed
Enrollment
2,000
Locations
1
Primary Endpoint
Genetic factors contributing to Chiari Type I malformation
OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Overview

Brief Summary

Duke University Medical Center is investigating the hereditary basis of Chiari type I malformations with or without syringomyelia (CM1/S). Our research is aimed at learning if CM1/S is indeed caused by factors inherited through the family and, if so, which genes are involved.

Study Design

Study Type
Observational
Observational Model
Family Based
Time Perspective
Cross Sectional

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Genetic factors contributing to Chiari Type I malformation

Time Frame: end of study

This study aims to identify genetic factors that contribute to or cause Chiari Type I malformation.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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