EFFECTS OF ESLICARBAZEPINE ACETATE (BIA 2-093) ON COGNITIVE FUNCTION IN CHILDREN WITH PARTIAL ONSET SEIZURES: AN ADD-ON, DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTICENTRE CLINICAL TRIAL - BIA-2093-208

BIAL - PORTELA & C?, S.A.0 个研究点目标入组 117 人开始时间: 2010年6月7日最近更新: 2015年12月28日

试验速览

阶段: 不适用
状态: 进行中（未招募）
发起方
入组人数: 117

研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

暂无简介。

研究设计

研究类型: Interventional clinical trial of medicinal product

入排标准

性别: All

入选标准

•1. Written informed consent signed by parent or legal representative and, where applicable, the patient. 2. Aged 6 to 16 years, inclusive. 3. A documented diagnosis of epilepsy for at least 12 months prior to screening. At least 2 partial onset seizures during the 4 weeks prior to screening despite treatment with 1 to 2 AEDs in a stable dose regimen. 4. An IQ of at least 70. 5. Current treatment with 1 to 2 AEDs (any except oxcarbazepine, benzodiazepines other than clobazam and VNS). 6. Excepting epilepsy, judged to be in general good health based on medical history, physical examination and clinical laboratory tests. 7. In the opinion of the investigator, able to complete the CDR test battery. 8. In case of a girl of childbearing potential, patient presents a serum ß-hCG test consistent with a non gravid state and agrees to remain abstinent or use reliable contraception (if used, hormonal contraception must be combined with a barrier method) starting at screening and continuing until at least the PSV. At Visit 2 (randomisation), patient must have: 9. At least 2 partial-onset seizures during the 4-week baseline period prior to randomisation (documented in a diary). 10. In case of a girl of childbearing potential, patient presents a urine ß-hCG test consistent with a non-gravid state. 11. Stable dose regimen of concomitant AEDs during the 4 week baseline period. 12. Diaries satisfactorily completed by the patient or his/her caregiver during the baseline period. 13. Satisfactory compliance with the study requirements during the baseline period
•Are the trial subjects under 18? yes
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) no
•F.1.2.1 Number of subjects for this age range
•F.1.3 Elderly (>=65 years) no
•F.1.3.1 Number of subjects for this age range

排除标准

•. Only simple partial seizures with no motor symptomatology (classified as A2 4 according to the International Classification of Epileptic Seizures). 2. Primarily generalised seizures. 3. Known rapidly progressive neurological disorders (progressive brain disease; epilepsy secondary to progressive cerebral lesion). 4. Occurrence of seizures too close together to count accurately. 5. History of status epilepticus or cluster seizures (i.e., 3 or more seizures within 30 minutes) within the 3 months prior to screening. 6. Seizures of non-epileptic origin. 7. Lennox-Gastaut syndrome. 8. West syndrome. 9. Major psychiatric disorders. 10. Seizures of psychogenic origin within the last 2 years. 11. History of schizophrenia or suicide attempt. 12. History of attention deficit disorder or other diseases adversely affecting cognitive abilities. 13. Currently treated with oxcarbazepine, benzodiazepines other than clobazam (on a routine or chronic basis) and/or VNS. 14. Known hypersensitivity to carboxamide derivatives (oxcarbazepine or carbamazepine). 15. Uncontrolled cardiac, renal, hepatic, endocrine, gastrointestinal, metabolic, haematological or oncology disorder. 16. Second or third degree atrioventricular blockade. 17. Relevant clinical laboratory abnormalities. 18. Estimated creatinine clearance (CLCR) <60 mL/min. 19. Pregnancy or nursing. 20. Treatment with ESL in any previous study. 21. Participation in other drug clinical trial within the last 2 months. 22. Not ensured capability to perform the trial. 23. Any other condition or circumstance that, in the opinion of the investigator, may compromise the patient s ability to comply with the study protocol. At Visit 2 (randomisation), patients must not be / have: 24. Any condition or circumstance that, in the opinion of the investigator, may compromise the patient s ability to comply with the study protocol

研究者

发起方

BIAL - PORTELA & C?, S.A.

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