- Trials with a EudraCT protocol (759)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
759 result(s) found for: Respiratory Tract Diseases AND Thoracic Diseases.
Displaying page 3 of 38.
EudraCT Number: 2011-001824-39 | Sponsor Protocol Number: CMID001A2201 | Start Date*: 2013-05-08 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A randomized, double-blind, double-dummy, placebo-controlled, 3-period crossover study to evaluate the pharmacodynamics, pharmacokinetics, safety and tolerability of orally inhaled indacaterol admi... | ||||||||||||||||||
Medical condition: Persistent Asthma | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-005365-39 | Sponsor Protocol Number: OR00213 | Start Date*: 2014-03-20 | ||||||||||||||||
Sponsor Name:Research in Real-Life Ltd | ||||||||||||||||||
Full Title: A guideline approach to therapy step-down utilising Flutiform®: change and step-down (FFLU-X study) | ||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001109-99 | Sponsor Protocol Number: SPON1595-17 | Start Date*: 2018-06-29 | ||||||||||||||||
Sponsor Name:Cardiff University | ||||||||||||||||||
Full Title: A randomised, placebo controlled trial of azithromycin for the prevention of chronic lung disease of prematurity in preterm infants | ||||||||||||||||||
Medical condition: Bronchopulomary dysplasia | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001376-15 | Sponsor Protocol Number: VPM1002-DE-3.06CoV | Start Date*: 2020-05-13 | |||||||||||
Sponsor Name:Vakzine Projekt Management GmbH | |||||||||||||
Full Title: A phase III, double-blind, randomized, placebo-controlled multicentre clinical trial to assess the efficacy and safety of VPM1002 in reducing healthcare professionals’ absenteeism in the SARS-CoV-2... | |||||||||||||
Medical condition: infectious respiratory diseases (e.g. COVID-19) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001278-31 | Sponsor Protocol Number: DEXA-COVID19 | Start Date*: 2020-04-01 | |||||||||||
Sponsor Name:Centro de Investigación Biomédica en Red Enfermedades Respiratorias (CIBERES) | |||||||||||||
Full Title: A comparative, randomised controlled trial for evaluating the efficacy of dexamethasone administration in the treatment of patients affected by COVID-19 with Acute Respiratory Distress Syndrome | |||||||||||||
Medical condition: Acute respiratory distress syndrome (ARDS) in patients affected by COVID-19 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002547-94 | Sponsor Protocol Number: 2011-420 | Start Date*: 2013-03-25 | ||||||||||||||||
Sponsor Name:Dept. of Intensive Care 4131, Rigshospitalet | ||||||||||||||||||
Full Title: Early Goal-Directed Nutrition in ICU Patients – EAT-ICU Trial | ||||||||||||||||||
Medical condition: Acutely admitted, mechanically ventilated intensive care unit patients. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002567-57 | Sponsor Protocol Number: 1.0 | Start Date*: 2020-11-23 | |||||||||||
Sponsor Name:University of Oxford / Clinical Trials and Research Governance | |||||||||||||
Full Title: To determine whether administration of almitrine bismesylate can ameliorate hypoxaemia in Covid-19 and augment effectiveness of supplementary oxygen therapy and respiratory support | |||||||||||||
Medical condition: Covid-19 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001244-26 | Sponsor Protocol Number: COV-2-SOLNATIDE-20 | Start Date*: 2020-04-11 | ||||||||||||||||
Sponsor Name:Department of Clinical Pharmacology, Medical University of Vienna, Vienna Austria | ||||||||||||||||||
Full Title: COVID-19: Efficacy of solnatide to treat pulmonary permeability oedema in SARS-Cov-2 positive patients with moderate-to-severe ARDS - a pilot-trial. | ||||||||||||||||||
Medical condition: Pulmonary permeability oedema in SARS-Cov-2 positive patients with moderate-to-severe ARDS | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020917-97 | Sponsor Protocol Number: ARC209 | Start Date*: 2010-06-23 | ||||||||||||||||
Sponsor Name:ASSOCIAZIONE ITALIANA PNEUMOLOGI OSPEDALIERI | ||||||||||||||||||
Full Title: SPHERIC-1 (Sildenafil in the Chronic Obstructive Pulmonary Disease associated to Chronic Pulmonary Hypertension. Sixteen weeks long, multicentre, randomized, double blind study, in comparison with ... | ||||||||||||||||||
Medical condition: Moderate to severe pulmonary hypertension associated to moderate to mild COPD. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002018-35 | Sponsor Protocol Number: ARC209/A | Start Date*: 2013-03-08 | ||||||||||||||||
Sponsor Name:ASSOCIAZIONE ITALIANA PNEUMOLOGI OSPEDALIERI | ||||||||||||||||||
Full Title: SPHERIC-1OE (Sildenafil and Pulmonary HypERtension In COPD – Open Extension) - A multicenter, longitudinal, 12 months open-label study, for the observation of the use of sildenafil in the treatment... | ||||||||||||||||||
Medical condition: Patients with pulmonary hypertension associated with chronic obstructive pulmonary disease enrolled in the study SPHERIC-1 | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001551-39 | Sponsor Protocol Number: 53718678RSV2005 | Start Date*: 2019-11-14 | |||||||||||
Sponsor Name:Janssen Sciences Ireland UC | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Clinical Outcomes, Antiviral Activity, Safety, Tolerability, Pharmacokinetics, and Pharmacokinetics/Pharmacodynamics of JNJ-5371... | |||||||||||||
Medical condition: Respiratory Syncytial Virus | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) SE (Completed) BE (Completed) BG (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001078-27 | Sponsor Protocol Number: 19999 | Start Date*: 2020-06-16 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: Safety and efficacy of inhaled pegylated adrenomedullin (PEG-ADM) in patients suffering from Acute Respiratory Distress Syndrome (ARDS): a double-blind, randomized, placebo-controlled, multicenter ... | |||||||||||||
Medical condition: Acute respiratory distress syndrome (ARDS) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Completed) AT (Prematurely Ended) IT (Prematurely Ended) GR (Prematurely Ended) NL (Prematurely Ended) BE (Completed) DK (Prematurely Ended) IE (Prematurely Ended) FI (Prematurely Ended) HU (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004152-19 | Sponsor Protocol Number: ELASTIC2011 | Start Date*: 2012-04-18 | |||||||||||
Sponsor Name:Ludwig Boltzmann institute for COPD and Respiratory Epidemiology | |||||||||||||
Full Title: Effects of ROFLUMILAST on markers of subclinical atherosclerosis In stable COPD; the ELASTIC-trial | |||||||||||||
Medical condition: chronic obstructive pulmonary disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-004079-17 | Sponsor Protocol Number: COMBATARF | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Efficacy and safety of 72-hour infusion of Prostacyclin (1 ng/kg/min) in mechanically ventilated patients with infectious pulmonary endotheliopathy – a multicentre randomized, placebo-controlled, b... | |||||||||||||
Medical condition: Infectious pulmonary endotheliopathy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003036-23 | Sponsor Protocol Number: 19SM5101 | Start Date*: 2019-12-02 | |||||||||||||||||||||||||||||||
Sponsor Name:Imperial College London | |||||||||||||||||||||||||||||||||
Full Title: Mechanisms of adverse effects of long-acting beta-agonists in asthma | |||||||||||||||||||||||||||||||||
Medical condition: Asthma | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002728-17 | Sponsor Protocol Number: GRC17536-204 | Start Date*: 2013-09-24 | |||||||||||
Sponsor Name:Glenmark Pharmaceuticals SA | |||||||||||||
Full Title: A Phase 2a, Multi-Centre, Randomised, Double-Blind, Parallel Group, Placebo-Controlled Study to Evaluate Efficacy, Safety and Tolerability of Inhaled GRC 17536, Administered for 4 Weeks, in Patient... | |||||||||||||
Medical condition: Refractory Chronic Cough. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003732-31 | Sponsor Protocol Number: CQAB149B2401 | Start Date*: 2012-01-23 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, 26-week study comparing the efficacy and safety of indacaterol (Onbrez® Breezhaler® 150 μg o.d.) with salmeterol/fluticasone propionate (Seretide® Accuha... | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004271-36 | Sponsor Protocol Number: FLUI-2011-77 | Start Date*: 2011-11-28 | |||||||||||
Sponsor Name:FluidDA nv | |||||||||||||
Full Title: Analysis of airway responses in severe COPD patients to Daxas®, using CT based functional respiratory imaging. | |||||||||||||
Medical condition: COPD = Chronic Obstructive Pulmonary Disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003162-12 | Sponsor Protocol Number: CSL312_2002 | Start Date*: 2022-05-02 | ||||||||||||||||
Sponsor Name:CSL Behring LLC | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Study to Investigate the Safety, Pharmacokinetics, and Pharmacodynamics of CSL312 in Subjects with Idiopathic Pulmonary Fibrosis | ||||||||||||||||||
Medical condition: Idiopathic Pulmonary Fibrosis | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) DK (Completed) AT (Completed) PL (Completed) IT (Completed) BE (Completed) ES (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001405-87 | Sponsor Protocol Number: GLPG1690-CL-303 | Start Date*: 2018-12-20 | |||||||||||
Sponsor Name:Galapagos NV | |||||||||||||
Full Title: A Phase 3, randomized, double-blind, parallel-group, placebo-controlled, multi-center study to evaluate the efficacy and safety of two doses of GLPG1690 in addition to local standard of care for mi... | |||||||||||||
Medical condition: Idiopatic pulmonary fibrosis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) DE (Prematurely Ended) BE (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) ES (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
