- Trials with a EudraCT protocol (580)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (39)
580 result(s) found for: Headache.
Displaying page 1 of 29.
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: 2018-003943-46 | Sponsor Protocol Number: 081018 | Start Date*: 2019-01-17 | |||||||||||
Sponsor Name:Danish Headache Center | |||||||||||||
Full Title: An open label study to evaluate the efficacy and tolerability of erenumab in the prophylactic treatment of persistent headache attributed to mild traumatic injury to the head | |||||||||||||
Medical condition: Post-traumatic headache | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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: 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: 2004-002737-39 | Sponsor Protocol Number: | Start Date*: 2005-06-14 |
Sponsor Name:National Headache Institute | ||
Full Title: Prophylactic treatment of episodic cluster headache with an angiotensin II receptor blocker (candesartan cilexetil); a randomized, placebo controlled parallel study. | ||
Medical condition: Episodic cluster headache | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
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: 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: 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: 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: 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: 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: 2015-005234-21 | Sponsor Protocol Number: I5Q-MC-CGAR | Start Date*: 2016-10-13 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3b Multicenter, Single-Arm, Open-Label Safety Study of LY2951742 (galcanezumab) in Patients with Episodic or Chronic Cluster Headache | |||||||||||||
Medical condition: Episodic Cluster Headache, Chronic Cluster Headache | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) FI (Completed) ES (Completed) DK (Completed) NL (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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: 2020-001968-28 | 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: 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: 2016-004213-28 | Sponsor Protocol Number: OTOBLOCKCH2016 | Start Date*: 2017-03-14 |
Sponsor Name:Department of Neuroscience, NTNU | ||
Full Title: Botulinum toxin type A block of the otic ganglion in chronic cluster headache. Safety issues. | ||
Medical condition: Cluster headache | ||
Disease: | ||
Population Age: Elderly | Gender: | |
Trial protocol: NO (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 (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2018-003148-21 | Sponsor Protocol Number: BASICstudy | Start Date*: 2019-01-25 |
Sponsor Name:NTNU- Norwegian University of Science and Technology | ||
Full Title: BASIC - Botulinum toxin type A blockade of the sphenopalatine ganglion in treatment-refractory chronic cluster headache | ||
Medical condition: Chronic cluster headache | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001969-37 | Sponsor Protocol Number: 19386A | Start Date*: 2021-03-05 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Interventional, randomized, double-blind, parallel-group, placebo-controlled delayed-start study to evaluate the efficacy and safety of eptinezumab in patients with episodic Cluster Headache | |||||||||||||
Medical condition: Episodic cluster headache | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) DK (Prematurely Ended) DE (Prematurely Ended) SE (Prematurely Ended) CZ (Completed) PT (Prematurely Ended) FR (Prematurely Ended) BE (Completed) NL (Prematurely Ended) FI (Completed) GR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006773-92 | Sponsor Protocol Number: FARM6TT8SP | Start Date*: 2008-07-23 | ||||||||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI PERUGIA | ||||||||||||||||||
Full Title: Sodium Valproate in the treatment of medication overuse headache: a controlled randomized clinical trial. | ||||||||||||||||||
Medical condition: medication overuse headache | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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