Rolandic Epilepsy Genomewide Association International Study
NCT03547050 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 210
Last updated 2023-10-06
Summary
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.
Conditions
- Rolandic Epilepsy
Interventions
- OTHER
-
Blood draw
Participation includes one visit for one blood draw per recruited patient. 10-20ml peripheral venous blood will be taken from the antecubital fossa. The DNA from the blood sample will then be extracted and resequenced for analysis.
- OTHER
-
Existing samples
Control DNA samples will be used that have been previously acquired in other studies.
Sponsors & Collaborators
-
King's College Hospital NHS Trust
collaborator OTHER -
Guy's and St Thomas' NHS Foundation Trust
collaborator OTHER -
Cardiff University
collaborator OTHER -
The Hospital for Sick Children
collaborator OTHER -
Hospital JP Garrahan
collaborator OTHER_GOV -
Aghia Sophia Children's Hospital of Athens
collaborator OTHER -
Hospital Mutua de Terrassa
collaborator OTHER -
Seattle Children's Hospital
collaborator OTHER -
Hasbro Children's Hospital
collaborator OTHER - collaborator OTHER
- lead OTHER
Eligibility
- Min Age
- 6 Years
- Max Age
- 25 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-06-01
- Primary Completion
- 2023-03-17
- Completion
- 2023-06-30
Countries
- United States
- Argentina
- Canada
- Greece
- Italy
- Spain
- United Kingdom
Study Locations
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