Result of tDCS in ASD Children With Comorbidities Like PANDAS, Rare Genetic Diseases or Autoimmune Disorders
Enrolling by invitation · Phase 1
Conditions studied: Attention, Visual Perceptual Weakness, Social Behavior, Fluency Disorder, EEG With Periodic Abnormalities
In brief
Results of the application of 100 sessions of tDCS for 12 months in children between 6 and 11 years old with autism spectrum disorder with rare diseases, genetic problems or PANDAS
Key facts
- Study ID
- NCT06368726
- Run by
- Spanish Foundation for Neurometrics Development
- People needed
- 180
- Starts
- 2024-04-01
- Expected to finish
- 2026-06-02
- Last updated by the study team
- 2026-05-19
Who can join
Age: 6 and older, up to 11. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age between 7 and 15 years old
- Diagnosis: PDD, ASD or PANDAS
- Have genetic alterations with geneticist reports like: mutation, random mating between organisms, random fertilization or crossing over (or recombination) between chromatids of homologous chromosomes during meiosis.
- Natural birth without caesarean or complications
- Normal Pregnancy
You may not qualify if…
- Head Trauma
- Brain Injuries like meningitis or encephalitis, including SaRS, Herpes or MERS infections
- Epilepsy
- Rare Diseases with Auto-Immune Disease
- Rare diseases with Endocrinology problems
- Fever or Biochemical problems in the First Blood Test (First Visit)
- Vaccines Reactions
Where it is running
- Bigdata4brain LLC — Albuquerque, New Mexico, United States
Full record on ClinicalTrials.gov
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