- 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 1 of 38.
EudraCT Number: 2009-014301-14 | Sponsor Protocol Number: 2009-014301-14 | Start Date*: 2009-07-15 | ||||||||||||||||||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | ||||||||||||||||||||||||||||
Full Title: Farmacologic prevention with Varenicline in heavy smokers undergoing early detection lung cancer screening | ||||||||||||||||||||||||||||
Medical condition: Heavy smokers with higher risk in developing lung cancer and smoke related diseases | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000620-14 | Sponsor Protocol Number: Cough/1/2010 | Start Date*: 2011-12-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA CAREGGI | |||||||||||||
Full Title: Effects of short term Erdosteine treatment on chronic cough on bronchitis phenotypes of COPD | |||||||||||||
Medical condition: COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002672-13 | Sponsor Protocol Number: CRHACS | Start Date*: 2021-03-18 | |||||||||||
Sponsor Name:ALMA MATER STUDIORUM UNIVERSITà DI BOLOGNA | |||||||||||||
Full Title: CPAP Reduces Hypoxemia After Cardiac Surgery (CRHACS Trial). A randomized controlled trial | |||||||||||||
Medical condition: Hypoxemia after cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002279-40 | Sponsor Protocol Number: OSAS_2011 | Start Date*: 2011-12-16 | |||||||||||
Sponsor Name:Med Uni Graz, Abt. für NEURO- u. GESICHTSCHIRURGISCHE ANÄSTHESIE u. INTENSIVMEDIZIN | |||||||||||||
Full Title: Comparative study of the hypnosedative management during video sleep endoscopy in patients with obstructive sleep apnoe syndrome | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003202-77 | Sponsor Protocol Number: NEOKOFF22 | Start Date*: 2023-04-04 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name: | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The effect of additional pre-extubational loading dose of caffeine-citrate | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Extubation failure and bronchopulmonary dysplasia | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: HU (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001675-33 | Sponsor Protocol Number: VPM1002-DE-3.07CoV | Start Date*: 2020-05-29 | |||||||||||
Sponsor Name:Vakzine Projekt Management GmbH | |||||||||||||
Full Title: A phase III, randomized, double-blind, placebo-controlled, multicentre, clinical trial to assess the efficacy and safety of VPM1002 in reducing hospital admissions and/or severe respiratory infecti... | |||||||||||||
Medical condition: infectious respiratory diseases (e.g. COVID-19) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006171-19 | Sponsor Protocol Number: 2011 | Start Date*: 2011-10-27 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MEYER | |||||||||||||
Full Title: randomized multicentric clinical trial upon efficacy of two different drugs combination to eradication of early p.aeruginosa infection in cystic fibrosis patients over 5 years old. | |||||||||||||
Medical condition: Cystic fibrosis patients with early P.aeruginosa infection. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000420-34 | Sponsor Protocol Number: PRISTL06562 | Start Date*: 2015-02-04 | |||||||||||
Sponsor Name:sanofi-aventis France | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000886-42 | Sponsor Protocol Number: BV-2020/08 | Start Date*: 2022-09-06 | |||||||||||
Sponsor Name:OM Pharma SA | |||||||||||||
Full Title: A Randomised, Placebo-Controlled, 3-Arm, Double-Blind, Multicentre, Phase 4 Study to Assess the Efficacy of OM-85 (Broncho Vaxom) Short- and Long-Term Treatment vs. Placebo in the Prevention of Res... | |||||||||||||
Medical condition: Respiratory Tract Infections with Wheezing Lower Respiratory Illness | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001294-25 | Sponsor Protocol Number: IPOXVILI | Start Date*: 2018-07-26 | |||||||||||||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO | |||||||||||||||||||||||
Full Title: Regional Hypo-perfusion as metabolic raiser of ventilator-induced lung injury (VILI): pilot clinica trial | |||||||||||||||||||||||
Medical condition: Severe Acute Respiratory Distress Syndrome (ARDS) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004534-23 | Sponsor Protocol Number: GATRA2016 | Start Date*: 2017-04-11 | |||||||||||||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO | |||||||||||||||||||||||
Full Title: Pilot study of Antithrombin supplementation during Extracorporeal Membrane Oxigenation | |||||||||||||||||||||||
Medical condition: Adult patients requiring veno-venous Extracorporeal circulation (ECMO) as a support for respiratory failure | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001849-41 | Sponsor Protocol Number: DOX-101 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:Leids Universitair Medisch Centrum (LUMC) | |||||||||||||
Full Title: Two-part, Randomized, Placebo-controlled, Repeated Stepped Infusion Dose Study of the Pharmacodynamics of Doxapram when Co-administered with Opioids (Protocol – doxapram-101). | |||||||||||||
Medical condition: acute respiratory insufficiency, including such conditions as opioid and anesthetic-induced respiratory depression, post-anesthetic atelectasis, and central apneas (e.g., apnea of prematurity). | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003519-40 | Sponsor Protocol Number: 03-CL-1202 | Start Date*: 2016-02-18 | |||||||||||||||||||||
Sponsor Name:Windtree Therapeutics, Inc | |||||||||||||||||||||||
Full Title: A MULTINATIONAL, MULTICENTER, MASKED, RANDOMIZED, CONTROLLED STUDY TO ASSESS THE SAFETY AND EFFICACY OF LUCINACTANT FOR INHALATION IN PRETERM NEONATES 26 TO 32 WEEKS GESTATIONAL AGE WITH RESPIRATOR... | |||||||||||||||||||||||
Medical condition: Respiratory Distress Syndrome (RDS) | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) IE (Completed) NL (Completed) HU (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005624-26 | Sponsor Protocol Number: 03-CL-1401 | Start Date*: 2016-05-30 | |||||||||||||||||||||
Sponsor Name:Windtree Therapeutics, Inc. (formerly Discovery Laboratories, Inc.) | |||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Open-Label, Controlled Trial to Assess the Safety and Tolerability of Lucinactant for Inhalation in Preterm Neonates 26 to 28 Weeks PMA. | |||||||||||||||||||||||
Medical condition: Respiratory Distress Syndrome (RDS) | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000106-32 | Sponsor Protocol Number: 03-CL-1702 | Start Date*: 2019-06-26 | |||||||||||||||||||||
Sponsor Name:Windtree Therapeutics, Inc. | |||||||||||||||||||||||
Full Title: A Multinational, Multicenter, Masked, Randomized, Parallel Group, Controlled Study to Assess the Safety and Efficacy of Lucinactant for Inhalation versus nCPAP alone in Preterm Neonates 26 to 32 We... | |||||||||||||||||||||||
Medical condition: Respiratory Distress Syndrome (RDS) | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000896-30 | Sponsor Protocol Number: Uni-Koeln-439 | Start Date*: 2009-02-09 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Surfactant application during spontaneous breathing with CPAP or during mechanical ventilation in the therapy of IRDS in premature infants <27 weeks | |||||||||||||
Medical condition: Idiopathic Respiratory Distress Syndrome (IRDS) in preterm infants | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000775-17 | Sponsor Protocol Number: PI11-0143 | Start Date*: 2012-11-21 | |||||||||||
Sponsor Name:Jesús Villar Hernández | |||||||||||||
Full Title: A comparative, randomised controlled trial for evaluating the efficacy of dexamethasone administration in the treatment of patients with the Acute Respiratory Distress Syndrome | |||||||||||||
Medical condition: Acute respiratory distress syndrome (ARDS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003897-30 | Sponsor Protocol Number: AERD-COV19 | Start Date*: 2022-05-30 | ||||||||||||||||
Sponsor Name:Jagiellonian University Medical College | ||||||||||||||||||
Full Title: Long-term aspirin therapy as a predictor of decreased susceptibility to SARS-CoV-2 infection in aspirin-exacerbated respiratory disease | ||||||||||||||||||
Medical condition: aspirin-exacerbated respiratory disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004854-27 | Sponsor Protocol Number: CFOR258D2416 | Start Date*: 2015-09-15 | |||||||||||
Sponsor Name:Novartis Pharma services AG | |||||||||||||
Full Title: A 26 week, randomized, active-controlled safety study of double-blind formoterol fumarate in free combination with an inhaled corticosteroid versus an inhaled corticosteroid in adolescent and adult... | |||||||||||||
Medical condition: Persistent asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) LT (Prematurely Ended) SE (Prematurely Ended) LV (Prematurely Ended) HU (Prematurely Ended) EE (Prematurely Ended) FI (Prematurely Ended) DK (Prematurely Ended) ES (Prematurely Ended) SK (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001406-29 | Sponsor Protocol Number: GLPG1690-CL-304 | Start Date*: 2019-01-28 | |||||||||||
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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) HU (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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