- Trials with a EudraCT protocol (580)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
580 result(s) found for: Dyspnea.
Displaying page 1 of 29.
EudraCT Number: 2019-003091-39 | Sponsor Protocol Number: APHP180158 | Start Date*: 2020-02-10 |
Sponsor Name:Assistance Publique des Hôpitaux de Paris | ||
Full Title: To relieve dyspnea with low dose titration of morphine in patients admitted to intensive care for acute respiratory failure: A pilot study - OPIDYS | ||
Medical condition: Adult patients admitted to intensive care for ARI: severe dyspnea (defined by a visual analogue dyspnea scale (EVA-dyspnea) ≥ 40) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000712-33 | Sponsor Protocol Number: 2008/001 | Start Date*: 2008-05-13 | |||||||||||
Sponsor Name:Medizinische Universität Graz | |||||||||||||
Full Title: Fentanyl for the treatment of dsypnea in patients with chronic heart failure | |||||||||||||
Medical condition: Symptomatic treatment of dyspnea induced by chronic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004412-22 | Sponsor Protocol Number: U-2013-007 | Start Date*: 2014-12-12 | |||||||||||
Sponsor Name:UCR Uppsala Clinical Research Center | |||||||||||||
Full Title: TRIAL OF CAFFEINE TO ALLEVIATE DYSPNEA RELATED TO TICAGRELOR (TROCADERO) A double-blinded, placebo-controlled, randomized, multicenter, development phase II study | |||||||||||||
Medical condition: Dyspnea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002533-22 | Sponsor Protocol Number: EB-1 | Start Date*: 2015-08-31 |
Sponsor Name:Aarhus University Hospital | ||
Full Title: Palliation of dyspnea with morphine in patients with interstitial lung disease | ||
Medical condition: Interstitial Lung disease | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-003784-15 | Sponsor Protocol Number: 2022_0422 | Start Date*: 2023-05-15 | |||||||||||
Sponsor Name:CHU DE LILLE | |||||||||||||
Full Title: Impact of inhaled BGF 160 on complexity and variability of tidal breathing and oscillatory mechanics in stable COPD patient. | |||||||||||||
Medical condition: Impact of inhaled BGF 160 on complexity and variability of tidal breathing and oscillatory mechanics in stable COPD patient | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021399-26 | Sponsor Protocol Number: CUERVO-07 | Start Date*: 2011-01-12 | ||||||||||||||||
Sponsor Name:Fundación para la Formación y la Investigación de los profesionales de la Salud (FUNDESALUD) | ||||||||||||||||||
Full Title: ENSAYO CLÍNICO CRUZADO PARA EVALUAR LA EFICACIA DEL TRATAMIENTO CON CITRATO DE FENTANILO ORAL TRANSMUCOSA DE LA DISNEA DE ESFUERZO EN PACIENTES CON CÁNCER AVANZADO | ||||||||||||||||||
Medical condition: Disnea de esfuerzo en pacientes con cáncer avanzado | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009579-36 | Sponsor Protocol Number: 26689 | Start Date*: 2009-10-20 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Effectiveness of inhaled corticosteroids in preschool children following hospital admission for acute dyspnea and wheeze | |||||||||||||
Medical condition: Dyspnea and wheeze in young children: Symptoms of dyspnea and wheeze occur frequently in young children. Most wheezing episodes in preschool children are associated with viral upper respiratory tra... | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021003-24 | Sponsor Protocol Number: 20100754 | Start Date*: 2011-07-28 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Safety and Efficacy of IV Infusion Treatment With Omecamtiv Mecarbil in Subjects With Left Ventricular Systolic Dys... | |||||||||||||
Medical condition: Acute heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GR (Completed) GB (Completed) LT (Completed) FI (Prematurely Ended) SK (Completed) CZ (Completed) HU (Completed) PL (Completed) BE (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001665-25 | Sponsor Protocol Number: 1 | Start Date*: 2018-10-23 |
Sponsor Name:Erasmus MC | ||
Full Title: Formoterol-beclomethasone in patients with bronchiectasis: a randomized, double-blind, placebo-controlled trial (Forza study) | ||
Medical condition: Bronchiectasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017082-39 | Sponsor Protocol Number: Bay 58-2667 / 14836 | Start Date*: 2010-02-01 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: A Placebo Controlled, Randomized, Double-Blind, Fixed-dose, Multicenter, Phase IIb Study to Investigate the Efficacy and Tolerability of BAY 58-2667 (50 μg/h, 100 μg/h, 150 μg/h) Given Intravenousl... | |||||||||||||
Medical condition: Acute Decompensated Chronic Congestive Heart Failure (ADHF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) IE (Prematurely Ended) ES (Prematurely Ended) DE (Prematurely Ended) FR (Completed) GB (Prematurely Ended) IT (Prematurely Ended) CZ (Prematurely Ended) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-004166-37 | Sponsor Protocol Number: 100424 | Start Date*: 2023-05-02 |
Sponsor Name:Division of Thoracic and Hyperbaric Surgery, Medical University Graz | ||
Full Title: Hyperbaric oxygenation for patients with orthostatic dysregulation (postural orthostatic tachycardia) in Long- COVID. Prospectively randomized cross- over study. | ||
Medical condition: Multiorgan symptoms after COVID-19 infection (Long COVID) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-002893-35 | Sponsor Protocol Number: CP027.2002 | Start Date*: 2013-11-21 |
Sponsor Name:Trevena Inc. | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Dose Ranging Study to Explore the Efficacy of TRV027 in Patients Hospitalized for Acute Decompensated Heart Failure | ||
Medical condition: Heart Failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) DE (Completed) CZ (Completed) SK (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003059-36 | Sponsor Protocol Number: Bay 58-2667/12480 | Start Date*: 2007-12-10 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: Placebo controlled, randomized, double-blind, multi-center, multinational Phase IIb study to investigate the efficacy and tolerability of BAY 58-2667 given intravenously in patients with acute deco... | |||||||||||||
Medical condition: Patients with acute decompensated chronic congested heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) IT (Prematurely Ended) SE (Prematurely Ended) EE (Prematurely Ended) CZ (Prematurely Ended) ES (Prematurely Ended) SI (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004899-35 | Sponsor Protocol Number: MORDYC | Start Date*: 2015-04-02 | |||||||||||
Sponsor Name:Maastricht University | |||||||||||||
Full Title: Morphine for palliative treatment of refractory dyspnea in patients with advanced COPD: benefits and respiratory adverse effects | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003971-16 | Sponsor Protocol Number: FEMODRIC | Start Date*: 2021-06-07 |
Sponsor Name:Fundació Assistencial Mútua Terrassa | ||
Full Title: A randomised, double-blind, comparative clinical trial of the effectiveness and tolerability of fentanyl in continuous parenteral perfusion versus on-demand bolus of morphine for the treatment of ... | ||
Medical condition: Refractory dyspnoea in patients hospitalised for acute decompensation of heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004064-11 | Sponsor Protocol Number: BETTER-BFeasibility | Start Date*: 2016-02-16 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: BETTER-B (Feasibility) BETter TreatmEnts for Refractory Breathlessness: A feasibility study of the use of mirtazapine for refractory breathlessness | |||||||||||||
Medical condition: Refractory breathlessness in patients diagnosed with cancer, chronic heart failure, or lung disease (chronic obstructive pulmonary disease (COPD) or interstitial lung disease (ILD)). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002403-13 | Sponsor Protocol Number: Ularitide-1502 | Start Date*: 2006-11-20 | |||||||||||
Sponsor Name:PDL BioPharma Inc | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blinded, Placebo-controlled Study of Ularitide in the Treatment of Subjects with Acute Decompensated Heart Failure | |||||||||||||
Medical condition: Acute decompensated heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) LT (Prematurely Ended) AT (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002695-45 | Sponsor Protocol Number: 15-156 | Start Date*: 2018-05-16 |
Sponsor Name:RWTH Aachen University represented by the Rector, himself, represented by the Dean of the Medical Faculty | ||
Full Title: Effect of Empagliflozin on Cardiac Output in Patients with Acute Heart Failure (EMPA Acute Heart Failure) | ||
Medical condition: Patients with acute heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
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: 2018-002466-39 | Sponsor Protocol Number: MVD-PROT-001 | Start Date*: 2019-04-17 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Morphine or Fentanyl for Refractory dyspnea in COPD | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease, COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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