- Trials with a EudraCT protocol (27)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
27 result(s) found for: Epilepsy surgery.
Displaying page 1 of 2.
EudraCT Number: 2014-004898-16 | Sponsor Protocol Number: V_1 | Start Date*: 2015-05-27 | |||||||||||
Sponsor Name:Medizinische Universität Wien | |||||||||||||
Full Title: A study to investigate (R)-11C-verapamil PET as a predictive biomarker for epilepsy surgery outcome | |||||||||||||
Medical condition: temporal lobe epilepsy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003381-27 | Sponsor Protocol Number: 100045 | Start Date*: 2018-09-24 |
Sponsor Name:CEA | ||
Full Title: Study in 18F-DPA714 PET to better locate preoperatively the epileptic focus to resect in drug-resistant partial epilepsy | ||
Medical condition: Brain imaging on people with partial pharmaco resistant epilepsy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005063-96 | Sponsor Protocol Number: HELLO-Study | Start Date*: 2007-11-13 | |||||||||||
Sponsor Name:University Hospital Tübingen | |||||||||||||
Full Title: Prospective trial of intravenous levetiracetam in patients with primary brain tumors and at least one symptomatic seizure who undergo biopsy or cytoreductive surgery. | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002455-25 | Sponsor Protocol Number: BIA-2093-304 | Start Date*: 2008-09-18 | |||||||||||
Sponsor Name:BIAL - Portela & Cª, SA | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ESLICARBAZEPINE ACETATE (BIA 2-093) AS ADJUNCTIVE THERAPY FOR REFRACTORY PARTIAL SEIZURES IN A DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED, PARALLEL-GROUP, MULTICENTRE CLINI... | |||||||||||||
Medical condition: simple partial seizures with no motor symptomatology Epilepsy | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Completed) DE (Completed) GR (Completed) CY (Completed) HU (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005971-18 | Sponsor Protocol Number: 13-617 | Start Date*: 2014-01-24 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: TimeToStop (TTS) Trial, A randomised controlled trial of early versus late antiepileptic drug withdrawal after pediatric epilepsy surgery | ||
Medical condition: We will investigate possible cognitive benifits of early antiepileptic drug withdrawal after pediatric epilepsy surgery. The concerning medical condition is refractory epilepsy | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000490-13 | Sponsor Protocol Number: EstuEla2022 | Start Date*: 2023-01-09 |
Sponsor Name:OILS4CURE S.L | ||
Full Title: Treatment, with a full spectrum extract of cannabis, in refractory epilepsy associated with tuberous sclerosis complex (TSC) | ||
Medical condition: Refractory epilepsy in tuberous sclerosis complex | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003607-17 | Sponsor Protocol Number: Rasmusscell | Start Date*: 2023-01-12 |
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario de La Princesa | ||
Full Title: Phase I, open-label clinical trial to evaluate the safety and clinical response of repeated-dose intra-arterial infusion of autologous mesenchymal cells in children and adolescents with refractory ... | ||
Medical condition: Autoimmune refractory epilepsy and Rasmussen Encephalitis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005065-64 | Sponsor Protocol Number: CBGG492A2202 | Start Date*: 2009-03-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, double-blind, randomized, placebo-controlled, two-arm parallel-group study of BGG492 as monotherapy in individuals with refractory partial seizures undergoing inpatient evaluation fo... | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002616-13 | Sponsor Protocol Number: Unknown | Start Date*: 2018-03-14 |
Sponsor Name:Maastricht Universitair Medisch Centrum | ||
Full Title: The effect of perioperative intravenous s-ketamine on acute and chronic postoperative craniotomy pain compared to placebo | ||
Medical condition: Post operative craniotomy pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004944-12 | Sponsor Protocol Number: E2080-A001-301 | Start Date*: 2017-03-14 |
Sponsor Name:Eisai Inc. | ||
Full Title: A Double-Blind, Placebo-Controlled, Parallel-Group Study of Rufinamide Given as Adjunctive Therapy in Patients with Refractory Partial Seizures | ||
Medical condition: Refractory partial seizures | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2006-000987-10 | Sponsor Protocol Number: N01235 | Start Date*: 2006-07-27 | |||||||||||
Sponsor Name:UCB S.A. [...] | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomized efficacy and safety study of levetiracetam extended release formulation (LEV XR), administered as 2 x 500 mg LEV XR tablets once daily as add-on thera... | |||||||||||||
Medical condition: Refractory epilepsy suffering from partial onset seizures | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000200-40 | Sponsor Protocol Number: N01148 | Start Date*: 2004-11-25 | |||||||||||
Sponsor Name:UCB Pharma S.A. [...] | |||||||||||||
Full Title: A Multi-Center, Open-Label, Long-Term, Follow-Up Study Of The Safety And Efficacy Of Levetiracetam In Children With Partial Onset Seizures. | |||||||||||||
Medical condition: Epilepsy - Refractory Partial Onset Seizures | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) BE (Completed) IT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003372-13 | Sponsor Protocol Number: EP0100 | Start Date*: 2023-11-17 |
Sponsor Name:UCB Japan Co. Ltd. | ||
Full Title: An Open-Label, Single-Arm, Multicenter Study of Levetiracetam as Monotherapy or Adjunctive Treatment of Partial Seizures in Pediatric Epileptic Subjects Ranging from 1 Month to Less Than 4 Years of... | ||
Medical condition: Partial Seizures | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2004-000199-14 | Sponsor Protocol Number: N01009 | Start Date*: 2004-11-25 | |||||||||||
Sponsor Name:UCB Pharma S.A. [...] | |||||||||||||
Full Title: A double-blind, randomized, multicenter, placebo-controlled, in-patients maximum 34 day study of levetiracetam oral solution (20-50 mg/kg/day) as adjunctive treatment of refractory partial onset se... | |||||||||||||
Medical condition: Epilepsy - Refractory Partial Onset Seizures | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) BE (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003702-26 | Sponsor Protocol Number: E2007-G000-208 | Start Date*: 2007-01-10 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Explore the Safety And Tolerability of Doses of E2007 up to a Maximum of 12 mg In Patients with Refractory Partial Seizures | |||||||||||||
Medical condition: Refractory Partial Seizures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) LV (Completed) EE (Completed) LT (Completed) BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000860-90 | Sponsor Protocol Number: CRAD001M2304 | Start Date*: 2013-02-14 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A three-arm, randomized, double-blind, placebo-controlled study of the efficacy and safety of two trough-ranges of everolimus as adjunctive therapy in patients with tuberous sclerosis complex (TSC)... | |||||||||||||
Medical condition: Refractory partial-onset seizures associated with tuberous sclerosis complex (TSC) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) NL (Completed) DE (Completed) HU (Completed) GB (Completed) BE (Completed) GR (Completed) DK (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006301-10 | Sponsor Protocol Number: MAGNA | Start Date*: 2012-05-10 | ||||||||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: Perioperative Magnesium Sulphate as a cerebral protector in neurosurgical patients | ||||||||||||||||||
Medical condition: Patient who are going to be under cerebral parenchyma resection, due to epilepsy or tumor | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004199-18 | Sponsor Protocol Number: E2007-A001-206 | Start Date*: 2006-03-22 |
Sponsor Name:Eisai Limited | ||
Full Title: A Double-blind, Placebo-controlled, Dose-escalation, Parallel Group Study of E2007 given as Adjunctive Therapy in Patients with Refractory Partial Seizures | ||
Medical condition: E2007 is given as adjunctive therapy in patients with refractory partial seizures | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) LT (Completed) DE (Completed) GB (Completed) ES (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003916-19 | Sponsor Protocol Number: 001 | Start Date*: 2015-12-30 |
Sponsor Name:Karl Landsteiner Institut für klinische Neurologie und Neuropsycholigie | ||
Full Title: Perioperative Levetiracetam for seizure prophylaxis in brain tumor patients. Prospective evaluation of side effects and efficacy | ||
Medical condition: Data on perioperative seizure prophylaxis in brain tumor patients as weil as on specific side effects is limited in scientific literature. Epileptic seizures during and after brain tumor surgery ma... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004552-37 | Sponsor Protocol Number: 18CH052 | Start Date*: 2019-05-07 | |||||||||||
Sponsor Name:CHU SAINT-ETIENNE | |||||||||||||
Full Title: Dose Study of Tranexamic Acid in Total Hip Replacement to Reduce Postoperative Hemoglobin Loss. A Phase 2 Randomized Double-blind Monocentric Study | |||||||||||||
Medical condition: Arthropathy of Hip | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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