- Trials with a EudraCT protocol (291)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (11)
291 result(s) found for: Pulmonary artery.
Displaying page 3 of 15.
EudraCT Number: 2020-002788-80 | Sponsor Protocol Number: Uni-Koeln-4243 | Start Date*: 2020-09-09 | ||||||||||||||||
Sponsor Name:University of Cologne | ||||||||||||||||||
Full Title: An explorative study to assess the safety, tolerability, and efficacy of AZD4831 in the treatment of pulmonary arterial hypertension (PAH) (MPO-PAH) | ||||||||||||||||||
Medical condition: Group 1: Pulmonary arterial hypertension (PAH) Group 2: Postcapillary pulmonary hypertension | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001008-23 | Sponsor Protocol Number: RIOP-1 | Start Date*: 2014-09-26 | |||||||||||
Sponsor Name:The Newcastle Upon Tyne Hospital NHS Foundation Trust, Freeman Hospital | |||||||||||||
Full Title: Riociguat in patients with respiratory disease and hypoxia – a proof-of-concept study | |||||||||||||
Medical condition: Pulmonary hypertension WHO Group III (Pulmonary hypertension owing to lung disease and/or hypoxia): Chronic obstructive pulmonary disease(COPD); Pulmonary Fibrosis (PF). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003978-41 | Sponsor Protocol Number: A1481298 | Start Date*: 2016-10-13 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: A Phase 3, Multi-center, Open label Study To Investigate Safety, Efficacy, And Tolerability Of Sildenafil Citrate In Pediatric Patients With Pulmonary Arterial Hypertension | |||||||||||||
Medical condition: Pulmonary arterial hypertension | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015013-46 | Sponsor Protocol Number: AnaesthesiaResearch024 | Start Date*: 2009-12-14 |
Sponsor Name:Alfred Health | ||
Full Title: The ATACAS Trial: Aspirin and Tranexamic Acid for Coronary Artery Surgery Trial | ||
Medical condition: Coronary Artery Bypass Grafting | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001199-31 | Sponsor Protocol Number: 57231 | Start Date*: 2017-03-20 |
Sponsor Name: | ||
Full Title: Improving treatment of right ventricular failure in pulmonary hypertension patients. | ||
Medical condition: End stage right ventricular failure in pulmonary hypertension patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000353-26 | Sponsor Protocol Number: SAFE-SSPE | Start Date*: 2021-09-20 |
Sponsor Name:Bern University Hospital | ||
Full Title: Clinical Surveillance vs. Anticoagulation for Low-risk Patients with Isolated Subsegmental Pulmonary Embolism: A Multicenter Randomized Placebo-Controlled Non-Inferiority Trial | ||
Medical condition: Isolated subsegmental pulmonary embolism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000801-50 | Sponsor Protocol Number: TDE-PH-302 | Start Date*: 2007-02-19 | |||||||||||
Sponsor Name:United Therapeutics Corporation | |||||||||||||
Full Title: A 12-Week, International, Multicenter, Double-Blind, Randomized, Placebo-Controlled Comparison of the Efficacy and Safety of Oral UT-15C Sustained Release Tablets in Subjects with Pulmonary Arteria... | |||||||||||||
Medical condition: Idiopathic or Familial pulmonary arterial hypertension (PAH), including PAH associated with: 1) Appetite suppressant/toxin use, or 2) Repaired congenital systemic-to-pulmonary shunts (repaired ≥... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) FR (Completed) BE (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002400-20 | Sponsor Protocol Number: 81866 | Start Date*: 2023-02-28 | |||||||||||
Sponsor Name:Amsterdam UMC, location VUmc | |||||||||||||
Full Title: Feasibility of empagliflozin as treatment for idiopathic pulmonary arterial hypertension | |||||||||||||
Medical condition: Idiopathic Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004999-53 | Sponsor Protocol Number: LTS10916 | Start Date*: 2009-02-06 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: Long-term safety study in patients included in CLARINET study with cyanotic congenital heart disease palliated with a systemic-to-pulmonary artery shunt and for whom the shunt is still in place at... | |||||||||||||
Medical condition: Patients at one year of age who are included in CLARINET, with cyanotic congenital heart disease palliated with a systemic-to-pulmonary artery shunt, and for whom the shunt is still in place. | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) HU (Completed) ES (Completed) BE (Completed) DE (Completed) FR (Completed) IT (Completed) GB (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010703-80 | Sponsor Protocol Number: AC-063A301 | Start Date*: 2009-06-11 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | |||||||||||||
Full Title: A Multicenter, Double-blind, Randomized, Placebo-controlled, Crossover Study to Assess the Effects of a Single Dose of Iloprost Power 15 on Exercise Capacity in Patients with Symptomatic Pulmonary ... | |||||||||||||
Medical condition: Indication: Symptomatic Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002692-33 | Sponsor Protocol Number: H6D-MC-LVGY | Start Date*: 2006-04-10 |
Sponsor Name:Lilly ICOS LLC | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Phase 3 Study of the Phosphodiesterase Type 5 (PDE5) Inhibitor Tadalafil in the Treatment of Patients with Pulmonary Arterial Hypertension | ||
Medical condition: Pulmonary arterial hypertension (PAH) is a chronic and progressive disease characterised by elevation of pulmonary artery pressure and pulmonary vascular resistance, leading to right heart failure ... | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) IE (Completed) DE (Completed) BE (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003514-14 | Sponsor Protocol Number: CL2-62798-010 | Start Date*: 2020-07-06 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: A Multicentre, Randomized, Double-blind, Placebo-controlled Dose-finding Study of S62798 in Patients with Intermediate-High Risk Acute Pulmonary Embolism on heparin | |||||||||||||
Medical condition: Acute intermediate high risk pulmonary embolism (PE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) GR (Prematurely Ended) PT (Completed) HU (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006072-32 | Sponsor Protocol Number: 2019/ABM/01/00078 | Start Date*: 2022-10-05 | |||||||||||
Sponsor Name:University Hospital in Poznań | |||||||||||||
Full Title: Pulmonary REsistance modification under treatment with Sacubitil/valsartaN in paTients with HeartFailure with reduced ejection fraction | |||||||||||||
Medical condition: Heart Failure with reduced ejection fraction. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003520-10 | Sponsor Protocol Number: BAY63-2521/12166 | Start Date*: 2006-10-20 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A multicenter, non-randomized, non-blinded, non-controlled study to investigate the impact of multiple doses of BAY 63 2521 on safety, tolerability, pharmacokinetics, and pharmacodynamics in patien... | |||||||||||||
Medical condition: Subjects with PH due to • Pulmonary arterial hypertension (PAH) [Venice protocol] or • Chronic thrombembolic PH (CTEPH) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000478-25 | Sponsor Protocol Number: MK-7962-008 | Start Date*: 2023-02-20 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: A Phase 2 Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Sotatercept (MK-7962) in Children from 1 to Less Than 18 Years of Age With PAH on Standard... | |||||||||||||
Medical condition: Pulmonary arterial hypertension | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) FR (Trial now transitioned) NL (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024585-22 | Sponsor Protocol Number: WILK3 | Start Date*: 2011-03-25 | |||||||||||
Sponsor Name:Imperial College Academic Healthsciences Centre | |||||||||||||
Full Title: What is the effect of intravenous iron supplementation on cardiopulmonary haemodynamics, exercise capacity and quality of life in patients with IPAH and iron deficiency? | |||||||||||||
Medical condition: Idiopathic or familial pulmonary arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000502-11 | Sponsor Protocol Number: EKOS-12 | Start Date*: 2016-07-21 |
Sponsor Name:EKOS Corporation | ||
Full Title: Study of the Optimum Duration of Acoustic Pulse Thrombolysis (APT) Procedure in the Treatment of Acute Submassive Pulmonary Embolism (OPTALYSE PE). | ||
Medical condition: Submassive pulmonary embolism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000134-22 | Sponsor Protocol Number: MDCO-CAN-15-01 | Start Date*: 2021-01-14 |
Sponsor Name:Chiesi Farmaceutici S.p.A. | ||
Full Title: A Prospective, Open-Label, Single-Arm, Multi-Center Study to Assess The Pharmacokinetics/Pharmacodynamics (PK/PD) AND Safety Of Different Cangrelor Doses In Neonatal Subjects At Risk Of Thrombosis. | ||
Medical condition: Postoperative neonatal cardiac subjects who are undergoing surgery for placement of systemic-to pulmonary artery palliative shunts (e.g., Blalock-Taussig or central shunt), right ventricle to pulmo... | ||
Disease: | ||
Population Age: Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000800-17 | Sponsor Protocol Number: TDE-PH-301 | Start Date*: 2007-02-15 | |||||||||||
Sponsor Name:United Therapeutics Corporation | |||||||||||||
Full Title: A 16-Week International, Multicenter, Double-Blind, Randomized, Placebo Controlled Comparison of the Efficacy and Safety of Oral UT-15C Sustained Release Tablets in Combination with an Endothelin... | |||||||||||||
Medical condition: Idiopathic or Familial pulmonary arterial hypertension (PAH), including PAH associated with: 1) Appetite suppressant use, or 2) Repaired congenital systemic-to-pulmonary shunts (repaired ≥ 5 yea... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) NL (Completed) AT (Completed) FR (Completed) BE (Completed) IT (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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