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NCT01858285Recruiting

Genetics of Epilepsy and Related Disorders

Source: ClinicalTrials.gov · Last updated 9 Jan 2026

Brief summary (registry, in English)

Investigators at Boston Children's Hospital are conducting research in order to better understand the genetic factors which may contribute to epilepsy and related disorders. These findings may help explain the broad spectrum of clinical characteristics and outcomes seen in people with epilepsy.

Status (registry)
Recruiting
Study type
Observational
Enrollment
5000 (estimated)
First submitted
9 May 2013
Start date
1 Nov 2010
Primary completion date
31 Dec 2030
Lead sponsor
Boston Children's Hospital
Diseases
Epilepsy
NCT number
NCT01858285

What you commit to

  • Study type: Observational
  • Planned participants: 5000
  • From 1 Nov 2010 to the primary completion date, 31 Dec 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • inclusion: diagnosis of epilepsy, patient at Boston Children's Hospital exclusion: existing genetic diagnosis or known cause for epilepsy, structural malformation of the brain, not seen at Boston Children's Hospital

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Boston Children's Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.