- Trials with a EudraCT protocol (280)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (20)
280 result(s) found for: Intranasal.
Displaying page 10 of 14.
EudraCT Number: 2018-004015-49 | Sponsor Protocol Number: FLU010 | Start Date*: 2019-03-14 | |||||||||||
Sponsor Name:Vaccitech Ltd | |||||||||||||
Full Title: Efficacy of MVA-NP+M1 in the influenza H3N2 Human Challenge model | |||||||||||||
Medical condition: influenza disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004226-16 | Sponsor Protocol Number: ACOT 2.0 | Start Date*: 2008-10-07 | |||||||||||
Sponsor Name:Carbylan BioSurgery, Inc. | |||||||||||||
Full Title: A prospective, multi-center, randomized, controlled, single-blinded study to evaluate the safety and efficacy of AdvaCoat Mx sinus gel for treatment of chronic rhinosinusitis without nasal polyps. | |||||||||||||
Medical condition: Subjects with chronic rhinosinusitis without nasal polyps, who have not had previous sinus surgery might be eligible for participation in this trial. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014982-16 | Sponsor Protocol Number: DIA002 | Start Date*: 2010-02-25 | |||||||||||
Sponsor Name:Wockhardt UK Limited | |||||||||||||
Full Title: An open label, single dose safety study of Diamorphine Hydrochloride Nasal Spray (0.1mg/kg) in children | |||||||||||||
Medical condition: The IMP is to be used as an analgesic for the relief of acute pain. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001591-11 | Sponsor Protocol Number: 3.4.11.049 | Start Date*: 2012-12-21 |
Sponsor Name:Erasmus MC | ||
Full Title: Symptomatic treatment of pollen related allergic rhinoconjunctivitis and the relation with asthma with children in the General practice | ||
Medical condition: Allergic Rhinitis Asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001459-35 | Sponsor Protocol Number: MC/PR/1400/007/11 | Start Date*: 2012-12-20 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: MULTICENTRE, RANDOMISED, DOUBLE-BLIND, PARALLEL GROUP, PLACEBO-CONTROLLED STUDY ON THE THERAPEUTIC EFFICACY AND SAFETY OF BECLOMETHASONE DIPROPIONATE SUSPENSION FOR INHALATION 800 micrograms TWICE... | |||||||||||||
Medical condition: Acute rhinosinusitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004917-10 | Sponsor Protocol Number: P05155 | Start Date*: 2015-03-03 |
Sponsor Name:Schering-Plough S.A. de C.V. | ||
Full Title: A Double-Blind Placebo-Controlled, Randomized, Parallel-Group, Multicenter Clinical Trial To Evaluate Efficacy And Safety Of Mometasone Furoate Nasal Spray In Children With Adenoid Hypertrophy. SNO... | ||
Medical condition: Adenoid Hypertrophy. | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-004921-41 | Sponsor Protocol Number: P06332 | Start Date*: 2015-02-24 |
Sponsor Name:Corporation Schering-Plough K.K. | ||
Full Title: Multicenter, double-blind, randomized, placebo-controlled study of mometasone furoate nasal spray in pediatric subjects with perennial allergic rhinitis | ||
Medical condition: perennial allergic rhinitis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2016-003107-65 | Sponsor Protocol Number: OPNT001-BN-001 | Start Date*: 2017-01-11 | |||||||||||
Sponsor Name:Opiant Pharmaceuticals Inc | |||||||||||||
Full Title: Randomised, double-blind, placebo controlled trial evaluating the effects of naloxone hydrochloride nasal spray on eating behaviours in bulimia nervosa | |||||||||||||
Medical condition: Bulimia nervosa | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022511-18 | Sponsor Protocol Number: X04 | Start Date*: 2011-04-05 | |||||||||||
Sponsor Name:Albert-Ludwig University Freiburg, Laboratory for Biological and Personality Psychology | |||||||||||||
Full Title: Behavioral effects and neural correlates of oxytocin on social attention [Verhaltenseffekte und neuronales Korrelat von Oxytocin im Kontext sozialer Aufmerksamkeit] | |||||||||||||
Medical condition: subjects with autism spectrum disorder and neurotypical controls | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002438-38 | Sponsor Protocol Number: HT-09 | Start Date*: 2012-02-21 | |||||||||||
Sponsor Name:Helperby Therapeutics Limited | |||||||||||||
Full Title: An open-label, multiple dose, efficacy study of HT61 in combination with marketed antibiotics, applied to the anterior nares in subjects with nasal carriage of Staphylococcus aureus (S. aureus). | |||||||||||||
Medical condition: Nasal carriage of Staphylococcus aureus (including MRSA) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002673-22 | Sponsor Protocol Number: 309189 | Start Date*: 2005-03-11 | |||||||||||
Sponsor Name:Schering AG | |||||||||||||
Full Title: Double-blind, placebo controlled, randomized, multicenter, parallel-group study to compare the efficacy and safety of Advantan cream twice weekly with Advabas cream during a maintenance phase of 16... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001682-33 | Sponsor Protocol Number: GB001-2101 | Start Date*: 2019-09-09 | |||||||||||
Sponsor Name:GB001, Inc. | |||||||||||||
Full Title: A Phase 2a, randomized, double-blind, placebo-controlled, multi-center study to evaluate the effect of GB001 in patients with chronic rhinosinusitis with or without nasal polyps | |||||||||||||
Medical condition: Chronic Rhinosinusitis with or without Nasal Polyps | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002877-23 | Sponsor Protocol Number: 1.0 | Start Date*: 2019-01-21 | |||||||||||
Sponsor Name:Abteilung für Neurologie der Medizinischen Universität Innsbruck | |||||||||||||
Full Title: Oxytocin and social attention in healthy controls and patients with Parkinson's disease. A randomised, double-blind, placebo-controlled, crossover eye tracking study. | |||||||||||||
Medical condition: Social functioning in Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004023-31 | Sponsor Protocol Number: LPS-Fluenz | Start Date*: 2016-01-06 |
Sponsor Name:Radboudumc | ||
Full Title: The effects of endotoxin challenge on the immune response elicited by a subsequent challenge with Fluenz™ in healthy volunteers, a pilot study | ||
Medical condition: Inflammatory conditions in general and immunosuppressive conditions is particular | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-006427-18 | Sponsor Protocol Number: 2021.143 | Start Date*: 2022-08-26 |
Sponsor Name:Anna Coquard Rafales | ||
Full Title: M-POC-O2: high flow nasal cannula oxygen versus conventional oxygen therapy in exacerbated chronic obstructive pulmonary disease (COPD) patients without respiratory acidosis. Pilot Study. | ||
Medical condition: Patients older than 35 years old with COPD diagnosis (chronic obstructive pulmonary disease) by spirometry, presenting acute exacerbation without respiratory acidosis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002470-42 | Sponsor Protocol Number: FluSHED-2 | Start Date*: 2018-08-30 | |||||||||||
Sponsor Name:Imperial College London JRC Office | |||||||||||||
Full Title: Assessment of viral shedding week following administration of live attenuated influenza vaccine in children: FluSHED-2 study | |||||||||||||
Medical condition: Prevention of influenza infection through immunisation | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000129-19 | Sponsor Protocol Number: NPY | Start Date*: 2015-08-28 | |||||||||||
Sponsor Name:Karolinska University Hospital, Huddinge | |||||||||||||
Full Title: A randomized , double-blind, placebo-controlled study of antidepressant effects of the endogen compound neuropeptide y (NPY) in patients suffering from major depressive disorder | |||||||||||||
Medical condition: Major depressive disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001601-82 | Sponsor Protocol Number: MR311-3506(AMBU-001) | Start Date*: 2019-07-08 |
Sponsor Name:Mundipharma Pharmaceuticals B.V. | ||
Full Title: Open randomized clinical trial to compare pain relief between low-dose methoxyflurane and standard of care for the treatment of patients with trauma pain in emergency medical services in the Nether... | ||
Medical condition: Patients with moderate trauma pain due to extremity injuries for whom the emergency medical services have been called. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000441-32 | Sponsor Protocol Number: REDOX2016 | Start Date*: 2016-10-27 |
Sponsor Name:Blekinge county council | ||
Full Title: REgistry-based randomized controlled trial of treatment Duration and mortality in long-term OXygen therapy (REDOX) A Multicenter, Phase III, Registry-Based, Randomized Controlled Trial (R-RCT) | ||
Medical condition: Chronic respiratory failure requiring LTOT (long-term oxygen treatment) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006088-61 | Sponsor Protocol Number: I8R-MC-IGBO | Start Date*: 2024-03-05 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: An Open-Label, Multi-Center, Single-Dose Study to Assess the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of Nasal Glucagon in Pediatric Patients with Type 1 Diabetes Aged 1 to <4 y... | ||
Medical condition: severe hypoglycemia | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
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