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The Genetics of Chiari Type I Malformation

NCT01060800 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2020-04-02

No results posted yet for this study

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.

Conditions

  • Chiari Type I Malformation

Sponsors & Collaborators

Principal Investigators

  • Allison Ashley-Koch, PhD · Duke University

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2017-04-25
Completion
2017-04-25

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01060800 on ClinicalTrials.gov