Rolandic Epilepsy Genomewide Association International Study

Completed

Conditions studied: Rolandic Epilepsy

In brief

We have discovered a small change in the genetic code which increases the risk of the brainwave abnormality that is found in rolandic epilepsy. We now wish to confirm this using a second much larger sample of patients. We will investigate the other genetic changes that cause people with the brainwave abnormality to develop seizures, as well as problems with speech, coordination, attention and learning.

Key facts

Study ID
NCT03547050
Run by
King's College London
People needed
210
Starts
2018-06-01
Expected to finish
2023-06-30
Last updated by the study team
2023-10-06

Who can join

Age: 6 and older, up to 25. 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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