Chiari Malformations
L
Laurie Ackerman, MD
Primary Investigator
Enrolling By Invitation
100 years and younger
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
-
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
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