The Genetics of Chiari Type I Malformation

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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01060800

Enrollment

2000

Registered

2010-02-02

Start date

2009-06-30

Completion date

2017-04-25

Last updated

2020-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chiari Type I Malformation

Keywords

Chiari, Chiari Type I, Chiari Type I Malformation, Familial Chiari

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.

Interventions

None listed

Study design

Observational model

FAMILY_BASED

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

The study is not currently enrolling new participants.

Design outcomes

Primary

Measure	Time frame	Description
Genetic factors contributing to Chiari Type I malformation	end of study	This study aims to identify genetic factors that contribute to or cause Chiari Type I malformation.

Countries

United States

Outcome results