- Trials with a EudraCT protocol (179)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
179 result(s) found for: Headaches.
Displaying page 1 of 9.
| EudraCT Number: 2004-000850-22 | Sponsor Protocol Number: 044(2A)SC04030 | Start Date*: 2004-09-17 | |||||||||||
| Sponsor Name:ANGELINI | |||||||||||||
| Full Title: Evaluation of tolerability and analgesic activity of paracetamol 1000 mg+caffeine 130 mg in the treatment of tension-type headache. Randomized, double blind, double-dummy, cross-over study vs. napr... | |||||||||||||
| Medical condition: Evaluation of tolerability and analgesic activity in the treatment of tension-type headache | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004436-34 | Sponsor Protocol Number: CSOM230Y2201 | Start Date*: 2017-02-06 | ||||||||||||||||
| Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
| Full Title: A Multicenter, Placebo-Controlled, Single Dose Study in Acute Episodic and Chronic Cluster Headache to Evaluate the Safety and Efficacy of SOM230 subcutaneous (s.c.) | ||||||||||||||||||
| Medical condition: Cluster headache | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2005-003505-85 | Sponsor Protocol Number: FHED-01 ANZ0009 | Start Date*: 2005-10-07 |
| Sponsor Name:Dermal Laboratories Limited | ||
| Full Title: 4head User Evaluation. | ||
| Medical condition: Tension-type headaches. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001763-23 | Sponsor Protocol Number: 2018-001763-23 | Start Date*: 2018-06-27 |
| Sponsor Name:Reinier van Arkel | ||
| Full Title: Treatment of headaches post-ECT with oxygen therapy; a proof of concept study | ||
| Medical condition: Headaches occuring after electro conculsion therapy. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001969-17 | Sponsor Protocol Number: VML 251-3MRM02 | Start Date*: 2005-01-10 |
| Sponsor Name:Vernalis Development Limited | ||
| Full Title: A double-blind, placebo-controlled, parallel group study, with an open-label extension phase, to assess the efficacy, tolerability and safety of oral frovatriptan in the prevention of menstrually-r... | ||
| Medical condition: Menstrually-Related Migraine (MRM) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Female | |
| Trial protocol: FI (Completed) SE (Completed) DE (Completed) GB (Completed) IT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-003846-97 | Sponsor Protocol Number: PS-2016-01 | Start Date*: 2016-12-08 | |||||||||||
| Sponsor Name:Section of Orofacial Pain and Jaw Function, Aarhus University | |||||||||||||
| Full Title: Phenotypic and genotypic characterization of a tension-type headache population | |||||||||||||
| Medical condition: Tension-type headache | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004399-16 | Sponsor Protocol Number: CHERUB01 | Start Date*: 2021-04-28 | |||||||||||
| Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
| Full Title: Efficacy of erenumab in chronic cluster headache: A 10-week double-blind, randomized, placebo-controlled, multicentric trial | |||||||||||||
| Medical condition: chronic cluster headache | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000149-22 | Sponsor Protocol Number: I5Q-MC-CGAL | Start Date*: 2015-07-02 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study of LY2951742 in Patients with Episodic Cluster Headache | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) DK (Completed) BE (Completed) FI (Completed) ES (Completed) NL (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005429-11 | Sponsor Protocol Number: I5Q-MC-CGAM | Start Date*: 2015-07-14 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study of LY2951742 with a Long-Term Open-Label Extension in Patients with Chronic Cluster Headache | |||||||||||||
| Medical condition: Chronic Cluster Headache | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) ES (Completed) DK (Completed) FI (Completed) BE (Completed) FR (Completed) NL (Completed) GR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019058-42 | Sponsor Protocol Number: LITIO-SUM-FC-002 | Start Date*: 2010-05-26 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | |||||||||||||
| Full Title: Safety of sumatriptan in combination with lithium for treatment of cluster headache, Pilot Study,Phase II | |||||||||||||
| Medical condition: Cluster Headache | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000248-91 | Sponsor Protocol Number: BTACH2012 | Start Date*: 2013-01-08 | |||||||||||
| Sponsor Name:Institutt for nevromedisin, NTNU | |||||||||||||
| Full Title: Endoscopic block of the sphenopalatine ganglion with botulinum toxin in intractable cluster headache. Safety issues. | |||||||||||||
| Medical condition: Pharmacological refractory cluster headache with durations of periods of attacks normally more than 2 months | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-006204-13 | Sponsor Protocol Number: PredCH | Start Date*: 2013-01-17 | |||||||||||
| Sponsor Name:University of Duisburg-Essen | |||||||||||||
| Full Title: Efficacy and safety of oral prednisone as add-on therapy in the prophylactic treatment of episodic cluster headache: a randomized, placebo controlled parallel study. | |||||||||||||
| Medical condition: Episodic Cluster Headache (ECH) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003729-62 | Sponsor Protocol Number: R-Verapamil-001 | Start Date*: 2013-01-16 | |||||||||||
| Sponsor Name:CENTER LABORATORIES, INC | |||||||||||||
| Full Title: A Randomized, Placebo-Controlled, Double-Blind, Parallel-Group, Phase 2 Study to Evaluate the Safety and Efficacy of R-Verapamil in the Prophylaxis of Episodic Cluster Headache | |||||||||||||
| Medical condition: Episodic Cluster Headache | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003736-38 | Sponsor Protocol Number: BIA-2093-209 | Start Date*: 2009-02-17 | |||||||||||
| Sponsor Name:BIAL-Portela & Ca, S.A. | |||||||||||||
| Full Title: Efficacy and safety of Eslicarbazepine acetate as preventive therapy for patients with migraine: a double-blind, randomised, placebo-controlled, parallel-group, multicentre clinical trial | |||||||||||||
| Medical condition: Adult patients with migraine with or without aura | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Completed) DE (Completed) AT (Completed) ES (Completed) PT (Completed) SK (Completed) CZ (Completed) BG (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002603-17 | Sponsor Protocol Number: H8H-MC-LAHX | Start Date*: 2020-08-04 |
| Sponsor Name:Eli Lilly and Company | ||
| Full Title: A Phase 1, Open-Label, Single-Dose Pharmacokinetic Study of Lasmiditan in Pediatric Patients With Migraine | ||
| Medical condition: Migraine | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2007-002435-93 | Sponsor Protocol Number: UNITHER/UN/07/001 | Start Date*: 2007-09-20 |
| Sponsor Name:UNITHER PHARMACEUTICALS | ||
| Full Title: Evaluation d'une solution hydro-alcoolique de sumatriptan administrée par voie sublinguale dans le traitement d'une crise d'algie vasculaire de la face, à la dose de 2mg, 4mg ou 6mg déterminée par ... | ||
| Medical condition: Cluster headaches | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-004999-36 | Sponsor Protocol Number: BCBe/04/FRO-CLU/001 | Start Date*: 2006-11-06 | |||||||||||
| Sponsor Name:Berlin-Chemie AG | |||||||||||||
| Full Title: Effects of Frovatriptan as Prophylactic Treatment of Cluster Headache, a Multi-Center, Placebo Controlled, Randomized, Double-Blind Prospective Phase III Parallel-Group Trial Comparing Frovatriptan... | |||||||||||||
| Medical condition: Episodic cluster headache | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001968-28 | Sponsor Protocol Number: 19385A | Start Date*: 2022-02-24 | |||||||||||
| Sponsor Name:H. Lundbeck A/S | |||||||||||||
| Full Title: Interventional, open-label, fixed-dose multiple administration study to evaluate long-term treatment with eptinezumab in patients with chronic cluster headache | |||||||||||||
| Medical condition: Chronic cluster headache | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) DK (Completed) NL (Completed) FI (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004351-23 | Sponsor Protocol Number: I5Q-MC-CGAS | Start Date*: 2021-02-22 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Study of Galcanezumab in Patients 6 to 17 Years of Age with Episodic Migraine – the REBUILD-1 Study | |||||||||||||
| Medical condition: Episodic Migraine | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) DE (Completed) IT (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001707-36 | Sponsor Protocol Number: 20120295 | Start Date*: 2014-02-26 | |||||||||||
| Sponsor Name:Amgen Inc. | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of AMG 334 in Chronic Migraine Prevention | |||||||||||||
| Medical condition: Prevention of chronic migraine | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) NO (Completed) FI (Completed) DK (Completed) PL (Completed) CZ (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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