Pediatric Movement Disorders of Unknown Etiology in Vietnam (VPeMD)

Recruiting now

Conditions studied: Movement Disorders in Children, Neuro Developmental Delay, Neurogenetic Disorders

In brief

This observational patient registry aims to describe the clinical phenotypes and genetic findings of Vietnamese children with movement disorders of unknown etiology. Eligible participants are children with clinically confirmed movement disorders after evaluation by pediatric neurology specialists and after exclusion of clear acquired causes. The study will collect clinical data, neurological examination findings, available laboratory and imaging results, and video recordings of abnormal movements when consent is provided. Blood samples will be collected for whole-exome sequencing and related genetic analysis. Genetic variants will be classified according to accepted clinical genetics standards and compared with the patients' clinical phenotypes. The study is expected to improve understanding of the phenotypic and genotypic spectrum of pediatric movement disorders in Vietnam, support genetic counseling, and evaluate how genetic results may influence diagnosis, follow-up, prognosis, and treatment planning.

Key facts

Study ID
NCT07695610
Run by
University of Medicine and Pharmacy at Ho Chi Minh City
People needed
50
Starts
2026-04-17
Expected to finish
2029-01-31
Last updated by the study team
2026-07-10

Who can join

Age: any, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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