The Genetics of Chiari Type I Malformation

Completed

Conditions studied: Chiari Type I Malformation

In brief

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.

Key facts

Study ID
NCT01060800
Run by
Duke University
People needed
2000
Starts
2009-06-01
Expected to finish
2017-04-25
Last updated by the study team
2020-04-02

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.