Clin2
NCT07755098Possibly a fitNot yet recruiting

Advanced genetic testing for unexplained intellectual disability

Intellectual DisabilityNeurodevelopmental Disorder (Diagnosis)srGSlrGSShort-read Genome SequencingLong-read Genome Sequencing

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

This study uses advanced genetic analysis to find the cause of unexplained severe intellectual disability or developmental disorders. It may help identify a diagnosis and guide care, even when standard genetic tests have been negative.

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

Phase
N/A
Enrollment
132 people
Ages
Any age
Study type
Interventional

Who can take part

  • You or your child have severe to profound intellectual disability or a syndromic neurodevelopmental disorder, meaning developmental delays along with other features.
  • Prior genetic testing (like a gene panel or exome) has been done and did not find a cause.
  • You and both biological parents can provide blood samples for testing. A skin biopsy (small skin sample) may also be needed from the affected person.
  • You and the parents must be able to give informed consent, and parents must be adults.
  • You must be covered by a social security or health insurance scheme.
  • The condition is not suspected to be caused by an injury, infection, or other acquired factor after birth.

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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