- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (160)
8 result(s) found for: Hydroxyzine.
Displaying page 1 of 1.
EudraCT Number: 2009-012340-16 | Sponsor Protocol Number: EPU P49 | Start Date*: 2009-07-20 |
Sponsor Name:Maastricht University | ||
Full Title: Effects of morning versus evening dose of hydroxyzine 50 mg on cognition in healthy subjects | ||
Medical condition: To assess the morning versus evening dose effect of hydroxyzine 50 mg on cognition in healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002890-37 | Sponsor Protocol Number: 1 | Start Date*: 2017-02-07 | |||||||||||
Sponsor Name:Esther Aleo Lujan | |||||||||||||
Full Title: Double-blind randomized clinical trial to compare presurgery anxiolysis in children treated with hydroxyzine versus non-pharmacological intervention (distractoria technique clown). | |||||||||||||
Medical condition: Presurgery anxiety | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022351-28 | Sponsor Protocol Number: 2010/38 | Start Date*: 2010-11-03 |
Sponsor Name:Hôpital FOCH | ||
Full Title: Essai prospectif randomisé, en double aveugle, comparant la Nalbuphine à l'association Hydroxyzine-Salbutamol dans la dystocie de démarrage. | ||
Medical condition: Dystocie de Démarrage | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003299-22 | Sponsor Protocol Number: BILA-3514/SCA | Start Date*: 2014-11-18 |
Sponsor Name:TNO.Netherlands Organization for Applied Scientific Research | ||
Full Title: Effects of Single Dose of Bilastine 20mg on Flying Ability in Healthy Volunteers Under Conditions of Simulated Cabin Pressure | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000426-66 | Sponsor Protocol Number: 29BRC18.0036 | Start Date*: 2018-07-13 | |||||||||||
Sponsor Name:CHRU de Brest | |||||||||||||
Full Title: Aprepitant versus Hydroxyzine en association avec les traitements cytoréducteurs pour les patients avec néoplasies myéloprolifératives souffrant d’un Prurit Aquagénique Persistant. | |||||||||||||
Medical condition: néoplasies myéloprolifératives avec Prurit Aquagénique Persistant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003940-21 | Sponsor Protocol Number: BILA-3918/PED | Start Date*: 2019-01-11 |
Sponsor Name:FAES FARMA, S.A. | ||
Full Title: A pilot, multicentre, single-blind, randomized, placebo-controlled, parallel-group clinical trial, to assess the safety of Bilastine treatment regarding psychomotor performance using a virtual real... | ||
Medical condition: Allergic rhinoconjunctivitis (both seasonal allergic rhinitis -SAR- and perennial allergic rhinitis -PAR-) and/or urticaria. | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015529-35 | Sponsor Protocol Number: 0918703 | Start Date*: 2009-12-04 | |||||||||||
Sponsor Name:CHU TOULOUSE | |||||||||||||
Full Title: Prise en charge pharmacologique de l’anxiété et de la douleur chez les patients qui souffrent en situation d’urgence traumatique préhospitalière : étude randomisée contrôlée en double-aveugle. | |||||||||||||
Medical condition: douleur en situation d’urgence traumatique préhospitalière | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001013-81 | Sponsor Protocol Number: ProBaBle | Start Date*: 2014-10-10 | |||||||||||
Sponsor Name:Centro Hospitalar de São João, EPE | |||||||||||||
Full Title: Treatment of Bladder Pain Syndrome with Onabotulinum toxin A | |||||||||||||
Medical condition: Bladder Pain Syndrome | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: PT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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