- Trials with a EudraCT protocol (1,305)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (121)
1,305 result(s) found for: Head.
Displaying page 1 of 66.
EudraCT Number: 2013-003707-18 | Sponsor Protocol Number: Evelien05 | Start Date*: 2014-04-22 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Absorption of sublingual delivered fentanyl (Abstral®) in head and neck cancer patients treated with curatively aimed chemo-radiotherapy | |||||||||||||
Medical condition: head and neck cancer patients treated with chemo-radiotherapy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001023-80 | Sponsor Protocol Number: 26 | Start Date*: 2015-02-09 | |||||||||||
Sponsor Name:Danish Head and Neck Cancer Group (DAHANCA) | |||||||||||||
Full Title: DAHANCA 26. A phase II unblinded, randomized study of paclitaxel and capecitabine with or without cetuximab as first line treatment of recurrent or metastatic squamous cell head and neck cancer (HN... | |||||||||||||
Medical condition: Recurrent or metastatic squamous cellular head and neck cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024046-29 | Sponsor Protocol Number: GEP 11/1010 | Start Date*: 2013-05-28 | |||||||||||
Sponsor Name:FNCLCC | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001641-40 | Sponsor Protocol Number: ESR-17-12933 | Start Date*: 2019-09-09 | ||||||||||||||||
Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | ||||||||||||||||||
Full Title: Induction Durvalumab (MEDI4736) & Radiotherapy (RT) for Locally Advanced but Resectable Head and Neck Squamous Cell Carcinomas: A Pilot Study | ||||||||||||||||||
Medical condition: Advanced resectable head and neck tumor | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001812-80 | Sponsor Protocol Number: 11-12-23/03-intern-6470 | Start Date*: 2011-11-25 | |||||||||||
Sponsor Name:Maastro Clinic | |||||||||||||
Full Title: Non invasive imaging of [18F]HX4 with Positron-Emission-Tomography (PET) in Head and Neck Cancer. | |||||||||||||
Medical condition: Patients with histological or cytological confirmed squamous cell carcinomas of the oral cavity, oropharynx, hypopharynx, larynx, T2-T3-T4, any N, M0 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017943-32 | Sponsor Protocol Number: 871 | Start Date*: 2010-05-31 | |||||||||||
Sponsor Name:Antwerp University Hospital | |||||||||||||
Full Title: Study of the combination of gemcitabine, cetuximab and radiotherapy in patients with head and neck cancer | |||||||||||||
Medical condition: Histologically confirmed squamous cell carcinoma of the head and neck which qualifies for definitive treatment with chemoradiation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002647-29 | Sponsor Protocol Number: ELECTROCHEMO-1 | Start Date*: 2014-02-12 | |||||||||||||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||||||||||||
Full Title: Clinical trial to evaluate the efficacy and tolerability of electrochemotherapy for palliative treatment in patients with head and neck squamous cell carcinoma | |||||||||||||||||||||||
Medical condition: head and neck squamous cell carcinoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001892-38 | Sponsor Protocol Number: CTPN01 | Start Date*: 2011-07-22 | |||||||||||
Sponsor Name:Panin S.r.l. | |||||||||||||
Full Title: A randomised, controlled, assessor-blind, clinical trial to compare Liceko ® with NIX/Lyclear 1% permethrin crème rinse in the treatment of head lice. | |||||||||||||
Medical condition: Head louse infestation (pediculosis capitis) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000257-23 | Sponsor Protocol Number: CTMK13 | Start Date*: 2011-06-14 | |||||||||||
Sponsor Name:Thornton & Ross Ltd | |||||||||||||
Full Title: A randomised, controlled, assessor-blind, clinical trial to demonstrate superiority of Hedrin® Once liquid gel compared with Lyclear 1% permethrin crème rinse in the treatment of head lice | |||||||||||||
Medical condition: Head louse infestation (pediculosis capitis) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013878-40 | Sponsor Protocol Number: 09.08 | Start Date*: 2009-08-24 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Phase II trial of Cetuximab in combination with chemotherapy (Carboplatinum and Navelbine) for patients with platinum-resistant head- and neckcancer | |||||||||||||
Medical condition: Platinum-resistant head and neck cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019804-21 | Sponsor Protocol Number: CTWE01 | Start Date*: 2010-05-18 | |||||||||||
Sponsor Name:Wepa Apothekenbedarf GmbH & Co KG | |||||||||||||
Full Title: A randomised, controlled, assessor-blind, clinical investigation of the activity of mosquito® LäuseShampoo compared with Infectopedicul® permethrin 0.5% lotion in the treatment of head lice | |||||||||||||
Medical condition: Infestation by head lice (pediculosis capitis) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004136-73 | Sponsor Protocol Number: CTMK05 | Start Date*: 2006-09-14 | |||||||||||
Sponsor Name:Thornton & Ross Limited | |||||||||||||
Full Title: A randomised, controlled, assessor-blind, clinical trial to demonstrate superiority of Hedrin 4% dimeticone lotion compared with Derbac-M 0.5% malathion aqueous liquid in the treatment of head lice | |||||||||||||
Medical condition: Head louse infestation | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004712-32 | Sponsor Protocol Number: UC-0130/1106 | Start Date*: 2012-01-10 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: A PHASE II, OPEN-LABEL, MULTICENTER TRIAL OF CABAZITAXEL IN PATIENTS WITH RECURRENT OR METASTATIC HEAD AND NECK CANCER AFTER FAILURE OF CISPLATIN, CETUXIMAB AND TAXANES. | |||||||||||||
Medical condition: Recurrent or metastatic head and neck cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006190-87 | Sponsor Protocol Number: CTOM01 | Start Date*: 2008-03-04 | |||||||||||
Sponsor Name:Omega Pharma N.V. | |||||||||||||
Full Title: A randomised, controlled, assessor-blind, clinical trial to investigate superiority of Lyclear spray away (ParaNix spray) compared with Infectopedicul permethrin 0.5% lotion in the treatment of hea... | |||||||||||||
Medical condition: Infestation by head lice (pediculosis capitis) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005787-13 | Sponsor Protocol Number: CTMK08 | Start Date*: 2008-10-27 | |||||||||||
Sponsor Name:Thornton & Ross Ltd | |||||||||||||
Full Title: A proof of concept clinical investigation to evaluate the activity of Hedrin 4% lotion in the treatment of head lice using a 1 hour application time | |||||||||||||
Medical condition: Head louse infestation (pediculosis capitis) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014737-24 | Sponsor Protocol Number: 68GaPET-HNSCC-2009 | Start Date*: 2010-11-19 | |||||||||||
Sponsor Name:Medizinische Universität Innsbruck | |||||||||||||
Full Title: Vergleichende Studie zur Darstellung der Somatostatinrezeptoren bei Kopf-Hals-Tumoren mit Immunhistochemie und PET (68Ga-DOTA-Tyr3-Octreotid) | |||||||||||||
Medical condition: Patients suffering from head and neck squamous cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004860-78 | Sponsor Protocol Number: P1209NY | Start Date*: 2014-05-09 | |||||||||||
Sponsor Name:G. Pohl-Boskamp GmbH & Co. KG | |||||||||||||
Full Title: A randomised, active-controlled, observer-blind, non-inferiority study to investigate the efficacy, safety and tolerability of a local treatment with dimeticone-based pediculicides in head lice inf... | |||||||||||||
Medical condition: Pediculosis capitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013317-10 | Sponsor Protocol Number: GEN211 | Start Date*: 2009-12-15 | |||||||||||
Sponsor Name:Genmab A/S | |||||||||||||
Full Title: An Open-label, Multi-Center, Phase I/II Trial Investigating the Pharmacokinetic profile of Zalutumumab, a Human Monoclonal Epidermal Growth Factor Receptor Antibody in non-curable patients with SCCHN | |||||||||||||
Medical condition: Non-Curable Squamous cell carcinoma of the head and neck (SCCHN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) GB (Prematurely Ended) HU (Completed) SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001928-29 | Sponsor Protocol Number: GORTEC2015-02 | Start Date*: 2015-07-07 | |||||||||||
Sponsor Name:GORTEC | |||||||||||||
Full Title: Phase II randomized trial comparating two concomitant administration of radiotherapy with cisplatin in patients with not operated or inoperable squamous cell carcinoma of the head and neck or with... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003636-36 | Sponsor Protocol Number: UCL/17/0396 | Start Date*: 2019-01-08 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: A phase II trial to assess the efficacy and safety profile of pembrolizumab in patients with performance status 2 with recurrent or metastatic squamous cell carcinoma of the head and neck | ||||||||||||||||||
Medical condition: Recurrent/metastatic head and neck squamous cell cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
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