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NCT05374928Completed

Human Epilepsy Project 3

Human Epilepsy Project 3: Newly Diagnosed Idiopathic Generalized Epilepsy

Source: ClinicalTrials.gov · Last updated 22 Jun 2026

Brief summary (registry, in English)

By carrying a careful, large-scale and ambitious prospective study of a cohort of participants with generalized epilepsy, the study team hopes to clarify the likelihood of response and remission in this type of epilepsy, and try to explore the underlying biological drivers of treatment response, including novel realms of exploration such as impact of the microbiome, and genetics. The identification of biomarkers that predict the likelihood of disease response would allow epilepsy patients to make more informed decisions about the factors affecting their quality of life, including plans for driving, relationships, pregnancy, schooling, work, and play. In addition to its impact on clinical care, the data and specimens collected in HEP3, including sequential electrophysiology, biochemical profiles and neuroimaging and banked DNA for future genomics studies, have the potential to provide new insights into the biological basis of IGE, thereby advancing the discovery of effective treatments and cures. By enrolling both newly diagnosed subjects (prognosis unknown) as well as subjects with established IGE who are already determined to be treatment resistant or treatment responsive, the study team can immediately test potential biomarkers in a confirmation cohort, which will accelerate identification of predictive biomarkers.

Status (registry)
Completed
Study type
Observational
Enrollment
316 (actual)
First submitted
11 May 2022
Start date
9 Mar 2020
Primary completion date
31 Dec 2025
Lead sponsor
NYU Langone Health
Diseases
Epilepsy
NCT number
NCT05374928

What you commit to

  • Study type: Observational
  • Participants enrolled: 316
  • From 9 Mar 2020 to the primary completion date, 31 Dec 2025
  • 18 sites in 2 countries
  • 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.

Prior treatment

  • History of previous or current significant psychiatric disorder that would interfere with study requirements
    • Cohort 2: Longstanding Treatment Responsive
  • History of previous or current significant psychiatric disorder that would interfere with study requirements
    • Cohort 3: Longstanding IGE, Treatment Resistant
  • History of previous or current significant psychiatric disorder that would interfere with study requirements
  • History of/suspicion of provoked seizures accounting for 25% or more of seizures over the prior 2 years (eg alcohol, non-adherence, significant sleep deprivation).

Other illness

  • Focal epilepsy
  • Generalized/focal epilepsy mixed syndromes
  • Progressive neurological disorder (brain tumor, Alzheimer's disease, progressive myoclonic epilepsy, etc.)
  • Major medical co-morbidities (e.g. renal failure requiring dialysis, metastatic cancer, HIV, or significant liver or renal disease)
  • Autism Spectrum Disorder
  • History of chronic drug or alcohol abuse (misuse or excessive use that interferes with activities of daily living) within the last 2 years
  • Seizures only during pregnancy
  • Focal epilepsy
  • Paroxysmal nonepileptic seizures
  • Generalized/focal epilepsy mixed syndromes
  • Progressive neurological disorder (brain tumor, Alzheimer's disease, progressive myoclonic epilepsy, etc.)
  • Major medical co-morbidities (e.g. renal failure requiring dialysis, metastatic cancer, HIV, or significant liver or renal disease)
  • Autism Spectrum Disorder
  • History of chronic drug or alcohol abuse (misuse or excessive use that interferes with activities of daily living) within the last 2 years
  • Seizures only during pregnancy
  • Focal epilepsy
  • Paroxysmal nonepileptic seizures
  • Generalized/focal epilepsy mixed syndromes
  • Progressive neurological disorder (brain tumor, Alzheimer's disease, progressive myoclonic epilepsy, etc.)
  • Major medical co-morbidities (e.g. renal failure requiring dialysis, metastatic cancer, HIV, or significant liver or renal disease)
  • Autism Spectrum Disorder
  • History of chronic drug or alcohol abuse (misuse or excessive use that interferes with activities of daily living) within the last 2 years
  • Seizures only during pregnancy

Other

  • Epileptic or developmental encephalopathy
  • Epileptic or developmental encephalopathy
  • Epileptic or developmental encephalopathy

Who the study is looking for

  • Age ≥13 years at time of enrollment
  • Age ≥8 years at time of seizure onset
  • Clinical seizure(s) and history consistent with IGE. The only permitted seizure types are absence, myoclonus or generalized tonic-clonic convulsions
  • Occurrence of at least 1 seizure of any type in the 6 months prior to treatment
  • Patients must have one of the following:
    • GTCSs alone accompanied by generalized spike-wave consistent with IGE per adjudication review
    • GTCSs with a history of absence and/or myoclonus, accompanied by generalized spike-wave consistent with IGE per adjudication review
    • GTCSs associated with a history of absence and/or myoclonus, not accompanied by generalized spike-wave consistent with IGE per adjudication review
    • A clear history of absence and/or myoclonus, accompanied by generalized spike-wave consistent with IGE per adjudication review
  • Availability of a complete medication history since initiation of treatment, including doses and date of initiation
  • No competing cause of epilepsy (e.g. traumatic brain injury)
  • AED treatment (for seizures) instituted not more than 12 months before enrollment
  • Age ≥13 years at time of enrollment
  • Age ≥8 years at time of seizure onset
  • Clinical seizure(s) and history consistent with IGE. The only permitted seizure types are absence, myoclonus or generalized tonic-clonic convulsions
  • Patients must have had one of the following:
    • GTCSs alone accompanied by generalized spike-wave consistent with IGE per adjudication review
    • GTCSs with a history of absence and/or myoclonus, accompanied by generalized spike-wave consistent with IGE per adjudication review
    • GTCSs associated with a history of absence and/or myoclonus, not accompanied by generalized spike-wave consistent with IGE per adjudication review
    • A clear history of absence and/or myoclonus, accompanied by generalized spike-wave consistent with IGE per adjudication review
  • Availability of a complete medication history since initiation of treatment, including doses and date of initiation
  • No competing cause of epilepsy (e.g. traumatic brain injury)
  • Two years of well-controlled seizures.
    • No convulsive seizures in the last two years
    • Myoclonic or absence seizures must be rare (\<2 per year) and non-disabling
    • Ongoing therapy with \> 1 antiseizure medication
  • Age ≥13 years at time of enrollment
  • Age ≥8 years at time of seizure onset
  • Clinical seizure(s) and history consistent with IGE. The only permitted seizure types are absence, myoclonus or generalized tonic-clonic convulsions
  • Occurrence of at least 1 seizure of any type in the 6 months prior to treatment onset
  • Patients must have had one of the following:
    • GTCSs alone accompanied by generalized spike-wave consistent with IGE per adjudication review
    • GTCSs with a history of absence and/or myoclonus, accompanied by generalized spike-wave consistent with IGE per adjudication review
    • GTCSs associated with a history of absence and/or myoclonus, not accompanied by generalized spike-wave consistent with IGE per adjudication review
    • A clear history of absence and/or myoclonus, accompanied by generalized spike-wave consistent with IGE per adjudication review
  • Availability of a complete medication history since initiation of treatment. This should include doses and date of initiation if possible, but minimum information would include name of drug, approximate duration of administration and reason for discontinuation, if applicable.
  • No competing cause of epilepsy (e.g. traumatic brain injury)
  • Treatment resistant IGE
    • Initiation of treatment at least 2 years prior to enrollment
    • Treatment resistance, as defined by failure of adequate trials of two tolerated and appropriately chosen and used AED schedules (whether as monotherapies or in combination to achieve seizure freedom). ASMs taken at enrollment would count towards this minimum.
    • Either or both of the following two:
    • One GTCC per year over the last 2 years. ii. Any type of seizure at least every 3 months which can consist of either: disabling myoclonus or absence (in the opinion of the subject and investigator) or GTCC d. Such seizures were not primarily due to significant illness (e.g, URI is not significant unless temperature \>101oF (38.3oC), nonadherence to antiseizure medications or \>2 alcoholic beverages within 48 hrs of seizure e. Ongoing therapy with \> 1 antiseizure medication

Criteria the registry did not label

  • Cohort 1: Newly Diagnosed IGE

Age in the registry: 13 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (18)

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

SiteCityCountrySite status
Monash University
Coordinator of this site? Confirm its status
MelbourneAustraliaUnknown status
The Johns Hopkins Hospital
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status
Mid-Atlantic Epilepsy Sleep Center
Coordinator of this site? Confirm its status
BethesdaUnited StatesUnknown status
St Barnabas Medical Center
Coordinator of this site? Confirm its status
LivingstonUnited StatesUnknown status
University of Miami
Coordinator of this site? Confirm its status
MiamiUnited StatesUnknown status
Yale University
Coordinator of this site? Confirm its status
New HavenUnited StatesUnknown status
NYU Langone Health - Comprehensive Epilepsy Center (CEC)
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Mount Sinai Hospital
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Northwell Health
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
University of Pennsylvania
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
Maine Medical Center
Coordinator of this site? Confirm its status
PortlandUnited StatesUnknown status
Mayo Clinic
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status
Minnesota Epilepsy Group
Coordinator of this site? Confirm its status
Saint PaulUnited StatesUnknown status
University of Utah Hospital
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesUnknown status
University of Texas Health Science Center
Coordinator of this site? Confirm its status
San AntonioUnited StatesUnknown status
University of California, San Francisco (UCSF)
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status
Washington University
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status
Georgetown University
Coordinator of this site? Confirm its status
Washington D.C.United StatesUnknown status

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