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Prospective Regional Epilepsy Database

Prospective Regional Epilepsy Database and Biobank for Individualized Clinical Treatment

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04559919
Acronym
PREDICT
Enrollment
1000
Registered
2020-09-23
Start date
2020-11-27
Completion date
2031-12-31
Last updated
2025-06-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epilepsy

Keywords

epilepsy, biomarker, access to care, quality of care, seizure

Brief summary

PREDICT is an observational study following adults with an unprovoked seizure or epilepsy in the health care region of western Sweden. The objective is to identify biomarkers and/or genetic predisposition of relevance for diagnosis and/or treatment of epilepsy and study the long-term prognosis and consequences of epilepsy.

Detailed description

Adults over 18 years of age, with an unprovoked seizure in the last year or epilepsy, resident in the health care region of western Sweden (VGR) at the time of inclusion. Baseline data and outcome variables are collected from several patient registries: the electronic medical records system in the health care region VGR and Swedish National Registers of healthcare, income, and employment managed by The National Board of Health and Welfare or Statistics Sweden, both of which are government agencies.

Interventions

OTHERSeizure status

We will collect information on first seizure ever, last seizure ever, number of seizure in last two months.

DIAGNOSTIC_TESTTests

We will collect results from imaging, electroencephalogram, and laboratory tests.

OTHEREpilepsy

We will collect information on risk factors of epilepsy, cause of epilepsy, epilepsy type/syndrome, medications tried, if the epilepsy is drug resistent, side effects of antiepileptic drugs.

OTHERDemographics and psychosocial

We will collect information on age, sex, date of death if applicable, marital status, education level, income type, driving status, employment, benefits, sick leave, number of household members.

OTHERHealth care

We will collect information on received health care; visit dates, caregiver, dispensation dates of antiepileptic drugs

Sponsors

Sahlgrenska University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Over 18 years of age * An unprovoked seizure within the last year or a diagnosis of epilepsy according to the current International League Against Epilepsy definition (epilepsy with seizure in the last ten or antiepileptic drug treatment in the last five years)

Exclusion criteria

* Expected survival less than two years * Inability to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
epilepsybaseline and years 1,2,3,4,5,6,7,8,9,10more than one seizure after first seizure
seizure statusbaseline and years 1,2,3,4,5,6,7,8,9,10the number of seizures in last two months and overall
drug resistant epilepsybaseline and years 1,2,3,4,5,6,7,8,9,10epilepsy that has not responded to two antiepileptic drugs
severe side effects of antiepileptic drugbaseline and years 1,2,3,4,5,6,7,8,9,10
psychosocial outcomesbaseline and years 1,2,3,4,5,6,7,8,9,10employment, marital status, income, sick leave

Secondary

MeasureTime frameDescription
received health carebaseline and years 1,2,3,4,5,6,7,8,9,10the number of visits for epilepsy, missed appointments, time intervals between visits

Countries

Sweden

Contacts

Primary ContactJohan Zelano, MD PhD
johan.zelano@vgregion.se+46313421000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 22, 2026