- Trials with a EudraCT protocol (26)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
26 result(s) found for: Nebulization.
Displaying page 1 of 2.
EudraCT Number: 2020-001700-42 | Sponsor Protocol Number: APHP200410 | Start Date*: 2020-05-06 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Efficacy of captopril nebulization in Covid-19 patients suffering of SARS-CoV-2 pneumonia. A randomized phase II study | |||||||||||||
Medical condition: Patient ≥18 with SARS Cov 2 pneumonia requiring oxygen administration. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000153-31 | Sponsor Protocol Number: AIR001-CS06 | Start Date*: 2013-01-22 |
Sponsor Name:Aires Pharmaceuticals, Inc | ||
Full Title: A Phase 2, Multi-Center, Open-Label study to evaluate the intermediate/long term safety and efficacy of AIR001 in subjects with WHO Group I Pulmonary Arterial Hypertension | ||
Medical condition: Pulmonary Arterial Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) DE (Completed) PL (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-001579-22 | Sponsor Protocol Number: OPTINEB | Start Date*: 2017-10-20 | |||||||||||
Sponsor Name:CHU DE POITIERS | |||||||||||||
Full Title: Effectiveness of nebulization by high nasal flow during acute respiratory decompensations of chronic respiratory insufficiency. | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000166-37 | Sponsor Protocol Number: AIR001-CS05 | Start Date*: 2013-01-22 |
Sponsor Name:Aires Pharmaceuticals Inc | ||
Full Title: A Phase 2, Multi-Center, Open-label, Randomized, Parallel-Dose Study to Determine the Safety and Efficacy of AIR001 in Subjects with WHO Group 1 Pulmonary Arterial Hypertension | ||
Medical condition: Pulmonary Arterial Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) PL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-002030-30 | Sponsor Protocol Number: AR_HSG_01-2008 | Start Date*: 2008-04-24 | |||||||||||
Sponsor Name:A.O. SAN GERARDO DI MONZA | |||||||||||||
Full Title: Impact of intraperitonael nebulization of local anesthetic on hypothermia and postoperative pain associated with laparoscopic surgery | |||||||||||||
Medical condition: Intra and post operatorive period | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018247-24 | Sponsor Protocol Number: AR HSG 01 2010 cholecysthectomy | Start Date*: 2010-03-04 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | |||||||||||||
Full Title: Peritoneal nebulization of Ropivacaine for postoperative pain control after laparoscopic cholecystectomy A multicentre, randomized, controlled, double blinded, phase III clinical trial; comparing... | |||||||||||||
Medical condition: Elective Laparoscopic cholecystectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002029-36 | Sponsor Protocol Number: AR_HSG_ 02-2008 | Start Date*: 2008-04-24 | |||||||||||
Sponsor Name:A.O. SAN GERARDO DI MONZA | |||||||||||||
Full Title: Impact of intraperitonael nebulization of local anesthetic on postoperative pain associated with laparoscopic cholecystectomy | |||||||||||||
Medical condition: Intra and post operatorive period | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004959-50 | Sponsor Protocol Number: Heliox-AP | Start Date*: 2016-05-29 | |||||||||||
Sponsor Name:S.E. Carburos Metálicos S.A. grupo Air Products | |||||||||||||
Full Title: HELIOX-DRIVEN BETA2-AGONISTS NEBULIZATION FOR CHILDREN WITH MODERATE TO SEVERE ACUTE ASTHMA: A RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: Moderate to severe exacerbations of asthma | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019830-29 | Sponsor Protocol Number: 3621 | Start Date*: 2011-04-19 | |||||||||||
Sponsor Name:Hopitaux Universitaires de Strasbourg | |||||||||||||
Full Title: Evaluation of the effects of CO2 insufflation on central body temperature and on postoperative pain in laparoscopic surgery | |||||||||||||
Medical condition: Elective videolaparoscopic hysterectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001892-34 | Sponsor Protocol Number: PI20208430041 | Start Date*: 2020-06-20 |
Sponsor Name:CHU Amiens-Picardie | ||
Full Title: Treatment of COVID-19 by Nebulization of Inteferon Beta 1b added to lopinavir/ritonavir: Feasibility, Efficiency and Safety Study | ||
Medical condition: Infection SARS-Cov-2 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018693-20 | Sponsor Protocol Number: AR HSG 02 2010 | Start Date*: 2010-03-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | |||||||||||||
Full Title: Do peritoneal nebulization of Ropivacaine reduce the use of morphine after short gynecologic laparoscopic surgery? A multicentre, randomized, controlled, double blinded, phase III clinical trial; ... | |||||||||||||
Medical condition: Elective ovarian cyst laparoscopic surgery | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021240-18 | Sponsor Protocol Number: ARHSG062010 | Start Date*: 2011-04-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. GERARDO DI MONZA | |||||||||||||
Full Title: Peritoneal nebulization of Ropivacaine for pain control after laparoscopic colectomy | |||||||||||||
Medical condition: Elective Laparoscopic colectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001713-20 | Sponsor Protocol Number: ASTHMAFAST | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Centre Hospitalier Intercommunal de Créteil | ||||||||||||||||||
Full Title: Comparison of the efficacy and safety of budesonide/formoterol Turbuhaler® versus terbutaline nebulization as reliever therapy in children with asthma presenting at the emergency room for moderate ... | ||||||||||||||||||
Medical condition: moderate asthma exacerbation | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003600-12 | Sponsor Protocol Number: 12001 | Start Date*: 2012-10-29 |
Sponsor Name:Sportmedisch expertisecentrum | ||
Full Title: The effect of cold air on the airways of elite skaters and the protective role of the OMRON | ||
Medical condition: Exericise induced bronchoconstriction | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-005014-21 | Sponsor Protocol Number: DPI-tobra-kind | Start Date*: Information not available in EudraCT |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Pharmacokinetic evaluation and tolerability of dry powder tobramycin via the Cyclops® in children with cystic fibrosis | ||
Medical condition: Cystic Fibrosis Lung infections | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002434-33 | Sponsor Protocol Number: Aprotinin1.0. | Start Date*: 2020-10-16 |
Sponsor Name:Hospital General Universitario Ciudad Real | ||
Full Title: Phase 3 randomized study to evaluate the safety and efficacy of aprotinin (Trasylol®) administered by inhalation nebulization in patients diagnosed with SARS-CoV-2 (COVID-19) with moderate severity... | ||
Medical condition: Patients with moderate SARS-CoV-2 pneumonia confirmed with a diagnosis of polymerase chain reaction (PCR) before randomization. The patient should be hospitalized and require ongoing medical care f... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002798-21 | Sponsor Protocol Number: WI18273 | Start Date*: 2005-02-18 |
Sponsor Name:F.Hoffmann-La Roche Ltd | ||
Full Title: A Phase II, prospective, randomized, double-blind, active-controlled, parallel group, multi-center 'proof of concept' trial in adult patients with community-acquired pneumonia requiring hospitaliza... | ||
Medical condition: Community-acquired pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LV (Completed) HU (Completed) SK (Completed) LT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001401-41 | Sponsor Protocol Number: TAPAS-2014 | Start Date*: 2014-07-29 |
Sponsor Name: | ||
Full Title: Targeting Antibiotics to Pseudomonas Aeruginosa in Small airways (TAPAS) study in patients with cystic fibrosis | ||
Medical condition: Cystic Fibrosis and chronic infection with Pseudomonas aeruginosa | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004315-13 | Sponsor Protocol Number: CIGE025AMX02 | Start Date*: 2017-05-08 |
Sponsor Name:Novartis | ||
Full Title: Multicentric, Open-label, Randomized, Parallel-group Study to Evaluate the Efficacy and Safety of Omalizumab in a 12-MonthPeriod, in Patients with Severe IgE-mediated Asthma Inadequately Controlled... | ||
Medical condition: Difficult to control severe asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2016-001054-17 | Sponsor Protocol Number: PHRN15-SE/AMIKINHAL | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:CHRU de Tours | |||||||||||||
Full Title: Double-blinded multicenter randomized controlled trial comparing inhaled amikacin versus placebo to prevent ventilator associated pneumonia | |||||||||||||
Medical condition: Patient with mechanical ventilation through an endotracheal tube | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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