Rolandic epilepsy-speech dyspraxia syndrome
MONDO:0015587A rare, genetic epilepsy characterized by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalized childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed.
9 clinical trials for this condition and its sub-types, 0 tagged with Rolandic epilepsy-speech dyspraxia syndrome itself.
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Browse by category →Sub-types of Rolandic epilepsy-speech dyspraxia syndrome
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Could a simple dental sealant plus remineralizer stop cavities in their tracks?
Disease control CompletedThis study tests two types of pit and fissure sealants (Fisseal and Prevent Seal) applied after treating teeth with one of two remineralizing agents (Biflourid or MI Paste). The goal is to see which combination best keeps the sealant in place and prevents cavities from forming or…
Sponsor: Ismail Dahshan • Aim: Disease control
Last updated Jul 17, 2026 00:00 UTC
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Routine EEGs may hold hidden clues to childhood epilepsy — a new analysis method is put to the test
Diagnosis CompletedThis study is testing whether a computer tool called BioEP can detect signs of seizure susceptibility in standard EEG recordings from children with epilepsy. Researchers will analyze past EEGs from 530 children aged 2 to 18 who already have an epilepsy diagnosis. The goal is to s…
Sponsor: Neuronostics Ltd • Aim: Diagnosis
Last updated Aug 01, 2026 00:00 UTC