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ZEBinix® Retention Rate in Epilepsy in Elderly Patients

ZEBinix Retention Rate in Epilepsy in Elderly Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04221282
Acronym
ZEBRE
Enrollment
50
Registered
2020-01-09
Start date
2019-04-01
Completion date
2020-09-30
Last updated
2020-01-09

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

Conditions

Aging, Aging Disorder, Epilepsy, Epilepsy; Seizure

Keywords

epilepsy, elderly, aging, zebinix, Eslicarbazepine acetate, tolerance, antiepileptic drug

Brief summary

The incidence of provoked and unprovoked seizures is known to increase with advancing age. Eslicarbazepine acetate (ESL) is one of the third generation of antiepileptic drugs (AEDs) that have been developed in the last ten years with a favorable safety profile. ESL is approved in Europe and the USA as adjunctive or monotherapy in adults with partial-onset seizures. Nevertheless, retrospective data in monotherapy condition in the elderly epileptic population are sparse. The aim of the ZEBRE study is to evaluate the efficacy and the safety of ESL in elderly epileptic patients (\> 65 years). The completion of this study will provide crucial information on the most appropriate ESL treatment for elderly patients suffering from partial seizures.

Detailed description

The ZEBRE (ZEBinix® Retention rate in epilepsy in Elderly patients) study is a prospective, multicenter, descriptive study. ESL will be prescribed according to the usual care. Posology and method of administration of ESL are defined by the summary of product characteristics.

Interventions

DRUGZebinix

ESL will be initiated by the investigator in patients as a first line monotherapy or adjunctive therapy. ESL will be prescribed according to the usual care. Posology and method of administration of ESL are defined by the summary of product characteristics. Then, data on the efficacy of ESL will be collected.

Sponsors

Centre Hospitalier Saint Joseph Saint Luc de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

1. Age ≥ 65 years 2. Ability of patient/legal representative to understand the study and to give his/her non-opposition (at the investigator's discretion) 3. Epilepsy with refractory partial-onset seizures with or without secondary generalization confirmed or with primary generalized tonic-clonic (PGTC) seizures 4. At least one seizure in the last three months 5. Treatment for partial-onset seizures with ESL as a first line monotherapy or with an adjunctive therapy

Exclusion criteria

1. History of ESL treatment 2. History of status epilepticus, seizures occurring in cluster, pseudo-seizures 3. History of severe hepatic impairment (aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \> 2 times ULN, gamma-glutamyltranspeptidase (GGT) \> 5 times ULN) 4. History of severe renal impairment (clearance CLCR \<30ml/min) 5. History of hypersensitivity to other carboxamide derivatives (e.g. carbamazepine, oxcarbazepine) 6. History of severe hyponatremia (\< 120 mmol/L) 7. Second or third degree atrioventricular block 8. More than one other antiepileptic drug

Design outcomes

Primary

MeasureTime frameDescription
Retention rate of ESL treatment as assessed by the number of patients that are still included in the study.at the end of the study treatment, at 6 monthsThe retention rate is representative of the effect of ESL since ESL will be pursued only if ESL has a sufficient efficacy without adverse effect. To evaluate the effect of ESL in elderly patients with partial-onset seizures, the retention rate will be measured after 6 months of treatment with ESL.

Secondary

MeasureTime frameDescription
Quality of life of patients as assessed by QoL-AD questionnaireat each visits required by the study (baseline, 3 months and 6 months)Some patients with epilepsy also have cognitive decline. QOL-AD (quality of life in Alzheimer'disease) measure quality of life in people with severe cognitive decline. A total score of 13-52, with higher scores indicating better QoL.
Quality of life of patients as assessed by NDDIE questionnaireat each visits required by the study (baseline, 3 months and 6 months)NDDI-E (neurological disorder depression inventory for epilepsy) is used for detecting major depressive disorder; a total score above 15 should raise the suspicion of a major depressive episode.
Quality of life of patients as assessed by QOLIE-10 questionnaireat each visits required by the study (baseline, 3 months and 6 months)QOLIE-10 (quality of life in epilepsy) is a quality of life questionnaire for adults with epilepsy. There are 10 questions about health and daily activities. All positive responses are lower numbers and all negative responses are higher numbers.
Incidence of seizures as assessed by the occurrence of seizuresat each visits required by the study (baseline, 3 months and 6 months)The number and the type of seizures or the number of seizure free in elderly patients will be reported
Observance of the treatment as recorded by the control of the drug administrationthrough study completion, an average of 6 monthsThe treatment delivery by the pharmacy be performed to assess the compliance of the treatment.
Incidence of treatment- adverse events as assessed by adverse events reportsthrough study completion, an average of 6 monthsNumber of patients with treatment-related adverse events will be reported to the pharmacovigilance department. Number of participants with abnormal laboratory values and/or adverse events that are related to treatment will be assessed.

Countries

France

Contacts

Primary ContactAdrien DIDELOT, MD, PhD
adidelot@ch-stjoseph-stluc-lyon.fr0033478616172

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026