Clin2
NCT05751525Possibly a fitRecruiting

Oral sulfonylurea study for children with KCNJ11-related delay and epilepsy

Neurodevelopmental DisordersIntellectual DisabilityDevelopment DelayADHDAutism Spectrum DisorderEpilepsy

Part of Brain & nervous system, Mental health clinical trials.

This study looks at whether switching to an oral sulfonylurea medicine can improve thinking, development, and seizure-related outcomes in children with a specific KCNJ11 gene change. You may be able to join if your child already has this mutation and has been able to take the medicine by mouth.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
21 people
Ages
2 years to 50 years
Study type
Observational

Who can take part

  • Your child is at least 2 years old
  • Your child has a specific KCNJ11 gene change called V59M (heterozygous)
  • Your child has already switched successfully to taking sulphonylurea by mouth
  • Your child is willing to take part in the study

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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