- Trials with a EudraCT protocol (263)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (12)
263 result(s) found for: Aura.
Displaying page 1 of 14.
| EudraCT Number: 2017-001288-18 | Sponsor Protocol Number: 16-API-01 | Start Date*: 2019-01-08 | |||||||||||
| Sponsor Name:CHU de Nice | |||||||||||||
| Full Title: ASIC channels and migraine disorders - Proof of concept study on the efficacy of Amiloride in prophylaxis of Migraine with Aura - APAM study | |||||||||||||
| Medical condition: Migraine with aura | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-010721-39 | Sponsor Protocol Number: NXN-188-202 | Start Date*: 2009-04-27 | |||||||||||
| Sponsor Name:Peer Tfelt-Hansen | |||||||||||||
| Full Title: A phase 2a Study of the Safety and Effectiveness of NXN-188 for the Acute Treatment of Migraine Attacks with Aura | |||||||||||||
| Medical condition: MIgraine with aura | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002470-27 | Sponsor Protocol Number: 3101-312-002 | Start Date*: 2021-05-12 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Allergan Limited | ||||||||||||||||||||||||||||||||||||||
| Full Title: A PHASE 3, MULTICENTER, OPEN-LABEL 52-WEEK EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY AND TOLERABILITY OF ORAL ATOGEPANT FOR THE PREVENTION OF MIGRAINE IN PARTICIPANTS WITH CHRONIC OR EPISODI... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Chronic or Episodic Migraine (Migraine without aura, migraine with aura, or chronic migraine) | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) CZ (Trial now transitioned) SE (Completed) HU (Trial now transitioned) DK (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2015-005689-40 | Sponsor Protocol Number: COL-MIG-302 | Start Date*: 2016-10-18 | |||||||||||||||||||||||||||||||
| Sponsor Name:CoLucid Pharmaceuticals, Inc. | |||||||||||||||||||||||||||||||||
| Full Title: A Study of Three Doses of Lasmiditan (50 mg, 100 mg and 200 mg) Compared to Placebo in the Acute TReaTment of MigrAiNe: A randomized, double-blind, placebo-controlled parallel group study (SPARTAN) | |||||||||||||||||||||||||||||||||
| Medical condition: acute migraine | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) DE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-005239-22 | Sponsor Protocol Number: BHV3000-404 | Start Date*: 2022-06-20 | |||||||||||||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||||||||||||
| Full Title: A Phase 4 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Rimegepant in Episodic Migraine Prevention with Multiple Dosing Regimens | |||||||||||||||||||||||
| Medical condition: Acute Migraine (with or without aura) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) AT (Completed) FR (Completed) SE (Completed) IT (Completed) PL (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2021-005246-15 | Sponsor Protocol Number: BHV3000-315 | Start Date*: 2022-08-23 | |||||||||||||||||||||
| Sponsor Name:Biohaven Pharmaceuticals Holding Company Limited | |||||||||||||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Rimegepant in Migraine Prevention in Children and Adolescents ≥ 6 to <18 years of age | |||||||||||||||||||||||
| Medical condition: Acute Migraine (with or without aura) | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) FR (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2015-005674-37 | Sponsor Protocol Number: COL-MIG-305(H8H-CD-LAHL) | Start Date*: 2016-11-01 | |||||||||||||||||||||||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||||||||||||||||||||||
| Full Title: An Open-label, LonG-term, Safety Study of LAsmiDItan (100 mg and 200 mg) in the Acute Treatment Of MigRaine (GLADIATOR) | |||||||||||||||||||||||||||||||||
| Medical condition: acute migraine | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) DE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-003761-18 | Sponsor Protocol Number: BHV3000-312 | Start Date*: 2022-01-20 | |||||||||||||||||||||||||||||||
| Sponsor Name:Biohaven Pharmaceuticals Inc. | |||||||||||||||||||||||||||||||||
| Full Title: Phase 3, multicenter, open-label study to assess the long-term safety and tolerability of rimegepant for the acute treatment of migraine (with or without aura) in children and adolescents ≥ 6 to < ... | |||||||||||||||||||||||||||||||||
| Medical condition: Acute Migraine (with or without aura) | |||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: ES (Ongoing) PL (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2006-000210-21 | Sponsor Protocol Number: TON/02/05-CLIN | Start Date*: 2006-03-27 |
| Sponsor Name:Prof Jes Olesen | ||
| Full Title: A single centre, double-blind, randomised, placebo controlled cross-over study to evaluate the efficacy and tolerability of tonabersat in the prophylaxis of migraine in patients presenting with mig... | ||
| Medical condition: Migraine with aura meeting the diagnostic criteria of the International Classification of Headache Disorders (Edition 2) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003517-35 | Sponsor Protocol Number: BHV3000-311 | Start Date*: 2021-05-05 | |||||||||||||||||||||||||||||||
| Sponsor Name:Pfizer, Inc. | |||||||||||||||||||||||||||||||||
| Full Title: Phase 3, multicenter, randomized, double-blind, group sequential, placebo-controlled study to assess efficacy and safety of rimegepant for the treatment of migraine (with or without aura) in childr... | |||||||||||||||||||||||||||||||||
| Medical condition: Acute Migraine (with or without aura) | |||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: SE (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-006207-36 | Sponsor Protocol Number: 19122011 | Start Date*: 2012-09-27 |
| Sponsor Name:Proreo Pharma Innovation AG | ||
| Full Title: A multi centre, double blind, randomised, placebo controlled crossover study to evaluate the efficacy and tolerability of picotamide in the prophylaxis of migraine in patients presenting with migra... | ||
| Medical condition: Migraine with aura, ICD-10NA G43.1 | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: HU (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-007336-17 | Sponsor Protocol Number: Version1.10 | Start Date*: 2009-08-06 |
| Sponsor Name:Medizinische Universität Wien, Uni. Klinik für Neurologie | ||
| Full Title: Blockade of the greater occipital nerve in frequent migraine and medication-overuse headache - a double-blinded, randomized, controlled trial | ||
| Medical condition: frequent migraine (defined at least 8 attacks per month) and medication-overuse headache | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-011009-18 | Sponsor Protocol Number: ALO-FC-001 | Start Date*: 2009-04-20 | ||||||||||||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | ||||||||||||||||||||||||||||
| Full Title: Pilot study on the efficacy of IV haloperidol in the treatment of chronic migraine with and without medication overuse | ||||||||||||||||||||||||||||
| Medical condition: Chronic migraine with and without medication overuse | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2020-000661-16 | Sponsor Protocol Number: CGRP2020 | Start Date*: 2020-06-18 | |||||||||||||||||||||
| Sponsor Name:Rigshospitalet Glostrup | |||||||||||||||||||||||
| Full Title: The effect of anti-calcitonin gene-related peptide (CGRP) receptor antibodies on the headache inducing properties of CGRP and cilostazol in migraine patients | |||||||||||||||||||||||
| Medical condition: Migraine | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2007-002654-36 | Sponsor Protocol Number: Zomig nasal 5mg/Imigran novum 100mg | Start Date*: 2007-10-08 |
| Sponsor Name:Carl Dahlöf | ||
| Full Title: A randomised prospective open multi-attack study of patient preference and efficacy between zolmitriptan nasal spray 5 mg and sumatriptan RDT 100 mg in the acute treatment of migraine. | ||
| Medical condition: Migraine with and without aura (G 43.0 and G 43.1) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004835-23 | Sponsor Protocol Number: TON/01/05-CLIN | Start Date*: 2006-01-26 |
| Sponsor Name:Minster Pharmaceuticals Ltd | ||
| Full Title: Multi-centre, parallel group, double-blind, placebo controlled study of the efficacy and tolerability of TONABERSAT in prophylaxis of migraine headache | ||
| Medical condition: Migraine with or without aura meeting the diagnostic criteria of the International Classification of Headache Disorders (Edition 2). | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: HU (Completed) DK (Completed) GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001989-15 | Sponsor Protocol Number: TV48125-MH-40142 | Start Date*: 2020-03-27 | ||||||||||||||||
| Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | ||||||||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study Followed by an Open-Label Extension to Evaluate the Efficacy and Safety of Fremanezumab for Preventive Treatment of... | ||||||||||||||||||
| Medical condition: Migraine and major depressive disorder (MDD) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) FR (Completed) FI (Completed) GR (Completed) ES (Ongoing) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-003223-30 | Sponsor Protocol Number: HeMiLa | Start Date*: 2017-08-14 |
| Sponsor Name:University Hospital Tübingen | ||
| Full Title: Prophylactic treatment of hemiplegic migraine with Lamotrigine | ||
| Medical condition: Familiar hemplegic migraine | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-006219-28 | Sponsor Protocol Number: MRSI | Start Date*: 2022-02-24 |
| Sponsor Name:Medical University Innsbruck | ||
| Full Title: MR-Spectroscopy: Investigating neurochemical changes in brain metabolism in migraineurs before and after CGRPAntibody treatment – a randomized, controlled, open-label trial | ||
| Medical condition: Episodic migraine | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-016375-30 | Sponsor Protocol Number: MK-0462-086 | Start Date*: 2010-02-16 | |||||||||||
| Sponsor Name:Merck & Co., Inc. | |||||||||||||
| Full Title: A Worldwide, Open Label, Clinical Trial to Examine the Long Term Safety and Tolerability of Rizatriptan in Pediatric Migraineurs for the Treatment of Migraine With or Without Aura | |||||||||||||
| Medical condition: Long term treatment of acute migraine, with or without aura, in children and adolescents, ages 12 to 17 years. | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) FI (Completed) DE (Completed) BE (Completed) ES (Prematurely Ended) EE (Completed) LV (Prematurely Ended) SE (Completed) FR (Prematurely Ended) PL (Prematurely Ended) DK (Completed) NO (Completed) GB (Prematurely Ended) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
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