Chiari Malformations

L
Laurie Ackerman, MD

Primary Investigator

Enrolling By Invitation
100 years or below
All
Phase N/A
100 participants needed
1 Location

Brief description of study

The aim of this study is to build a database of genetic, clinical and radiological information for individuals with Chiari Type I to learn more about this diagnosis.

Detailed description of study

After enrollment in the study, participants will be asked to complete a medical questionnaire, give a saliva sample, and give a blood sample.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: chiari malformation, syringomyelia, Riley
  • Age: 100 years or below
  • Gender: All

Inclusion Criteria:
  •  
  • Any individual having the diagnosis of Chiari I or Individuals who have a relative diagnosed with Chiari I malformation.
  • If under the age of 18, have a parent/legal guardian available to provide consent and assist in answering questions.
  • Speak and read English
  • Able to fill out questionnaire, or have a parent or proxy fill it out on their behalf.
Exclusion Criteria:
  •  
  • Individuals with Chiari I secondary to another preexisting diagnosis (e.g.: malignant brain tumor), and individuals with Myelomeningocele
  • Adults unable to give consent
 

Updated on 03 Nov 2024. Study ID: 1910649123, 201904099, SNEU-WASHU-CHIARI
Please visit our main page to search for other studies you may be interested in. If you need help finding a study or have any questions, please contact us at inhealth@iu.edu

Interested in the study?

This study is accepting only persons who receive care at a certain clinic or doctor or who are part of an invited group. Questions about this study can be directed to the study team listed in the description or contact your doctor to see if you are eligible.

Accepting Referrals by Invitation Only