Immunogenomic Analyses of Pediatric Catatonia

Rady Children's Institute for Genomic Medicine seeks to understand the genomes and immune systems in 40 children and adolescents who are admitted to Rady Children's Hospital San Diego with a catatonia diagnosis. Cutting-edge genome and protein sequencing technology will be used to better understand how immunological and genetic assessments may improve the ability to identify the cause of catatonia and impact care. The investigator also hopes to identify new genetic and/or autoimmune causes of catatonia that may inform new treatment for future patients.

NCT Number	NCT06656572
Lead Sponsor	Rady Pediatric Genomics & Systems Medicine Institute Collaborators: Brain & Behavior Research Foundation
Conditions	Catatonia
Enrollment	120 participants
Start Date	2024-12-01
Primary Completion	2026-09-01 (estimated)
Study Completion	2030-09-01 (estimated)
Updated on ClinicalTrials.gov	2024-11-14