Viewing Study NCT06593951

Home Icon Home Search Icon Search Certify Doc Icon Certify Doc Certify Doc Icon Genes Certify Doc Icon Clinical Trials Certify Doc Icon CompTox Processes Icon DrugMatrix Open Targets Icon Open Targets Processes Icon Products Support Icon Support Bugs Icon Bugs
Main Search Make This Study a Gene Therapy Make This Study a Not Gene Therapy Report Bug
Ignite Creation Date: 2025-12-24 @ 11:43 PM
Ignite Modification Date: 2026-02-10 @ 11:59 AM
Study NCT ID: NCT06593951
Status: RECRUITING
Last Update Posted: 2024-10-15
First Post: 2024-09-10
Is NOT Gene Therapy: True
Has Adverse Events: False
Brief Title: Registry and Natural History Study for Progressive Myoclonus Epilepsy Type 1 (EPM1)
Sponsor: Boston Children's Hospital
Organization:
Overview Dates Organization Conditions Design Enrollment Locations Outcomes Modules Raw JSON

Conditions & Keywords Data

Conditions:

Conditions

Condition Brief Condition Text View
None Progressive Myoclonus Epilepsy Type 1 View
None EPM1 View
None CSTB-related Disease View
None Myoclonus Epilepsies, Progressive View
None Unverricht-Lundborg Disease View
None Progressive Epilepsy and/or Ataxia With Myoclonus as a Major Feature View
None PME View
None Progressive Myoclonus-Epilepsies View
Keywords:

Keywords

Keyword Brief Keyword Text View
None Myoclonus View
None Progressive Myoclonus View
None CSTB View
None Non-epileptic action-induced myoclonus View
None Non-epileptic stimulus-induced myoclonus View
None Cerebellar disfunction View
None EPM1 View