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
Sites (18)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Monash University Coordinator of this site? Confirm its status | Melbourne | Australia | Unknown status |
| The Johns Hopkins Hospital Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| Mid-Atlantic Epilepsy Sleep Center Coordinator of this site? Confirm its status | Bethesda | United States | Unknown status |
| St Barnabas Medical Center Coordinator of this site? Confirm its status | Livingston | United States | Unknown status |
| University of Miami Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Yale University Coordinator of this site? Confirm its status | New Haven | United States | Unknown status |
| NYU Langone Health - Comprehensive Epilepsy Center (CEC) Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Mount Sinai Hospital Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Northwell Health Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| University of Pennsylvania Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| Maine Medical Center Coordinator of this site? Confirm its status | Portland | United States | Unknown status |
| Mayo Clinic Coordinator of this site? Confirm its status | Rochester | United States | Unknown status |
| Minnesota Epilepsy Group Coordinator of this site? Confirm its status | Saint Paul | United States | Unknown status |
| University of Utah Hospital Coordinator of this site? Confirm its status | Salt Lake City | United States | Unknown status |
| University of Texas Health Science Center Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
| University of California, San Francisco (UCSF) Coordinator of this site? Confirm its status | San Francisco | United States | Unknown status |
| Washington University Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
| Georgetown University Coordinator of this site? Confirm its status | Washington D.C. | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.