- Trials with a EudraCT protocol (164)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
164 result(s) found for: Pulmonary vascular disorders.
Displaying page 1 of 9.
| EudraCT Number: 2012-004583-22 | Sponsor Protocol Number: 548.12 | Start Date*: 2012-10-20 | |||||||||||
| Sponsor Name:OSPEDALE PEDIATRICO BAMBINO GESU' DI ROMA | |||||||||||||
| Full Title: Verification of the effectiveness of intravenous sildenafil compared to other pulmonary vasodilators used in the test vessel reactivity of pulmonary | |||||||||||||
| Medical condition: Subjects in children with congenital heart disease surgery or not, with echocardiographic signs of pulmonary hypertension followed at the Pediatric Cardiology Centre of the Mediterranean or reporte... | |||||||||||||
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| Population Age: In utero, Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000137-31 | Sponsor Protocol Number: 2017-2019 | Start Date*: 2017-12-19 | ||||||||||||||||
| Sponsor Name:VU University Medical Center | ||||||||||||||||||
| Full Title: Pulmonary Hypertension REversal in Clusters of Patients With Identical Pathobiological Substrates. 6-Mercaptopurine Proof-of-Concept Trial | ||||||||||||||||||
| Medical condition: Pulmonary arterial hypertension | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-003627-29 | Sponsor Protocol Number: PREVENTIHSSTUDY(FARM12L9JE) | Start Date*: 2017-02-22 | |||||||||||
| Sponsor Name:OSPEDALE SANTA MARIA DELLA MISERICORDIA | |||||||||||||
| Full Title: PREvention of VENous Thromboembolism In Hemorrhagic Stroke patients | |||||||||||||
| Medical condition: hemorrhagic stroke | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000709-38 | Sponsor Protocol Number: BBR | Start Date*: 2015-10-20 | |||||||||||
| Sponsor Name:Medical University of Graz | |||||||||||||
| Full Title: Acute Effects of Benzbromaron on the pulmonary circulation | |||||||||||||
| Medical condition: Pulmonary arterial hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001633-40 | Sponsor Protocol Number: ESRA | Start Date*: 2022-03-07 | |||||||||||
| Sponsor Name:Thoraxklinik Heidelberg gGmbH | |||||||||||||
| Full Title: Efficacy and safety of riociguat (MK-4836) in incipient pulmonary vascular disease as an indicator for early pulmonary arterial Hypertension Doubleblind, randomized, multicentre, multinational, pla... | |||||||||||||
| Medical condition: early pulmonary vascular disease, defined as either a) mean pulmonary arterial pressure (mPAP) ≥25 mmHg with pulmonary vascular resistance (PVR) ≥2 to <3 WU and pulmonary arterial wedge pressure (P... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017155-10 | Sponsor Protocol Number: 10-aifa-2005-01 | Start Date*: 2006-11-07 | |||||||||||
| Sponsor Name:CASA DI CURA PRIVATA S.RAFFAELE - PISANA | |||||||||||||
| Full Title: Evaluation of tolerability and efficacy of the combination Sildenafil/Bosentan in patients with severe pulmonary hypertension. | |||||||||||||
| Medical condition: severe pulmonary hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002835-17 | Sponsor Protocol Number: 250774 | Start Date*: 2016-01-18 | ||||||||||||||||||||||||||
| Sponsor Name:Justus Liebig Universität Gießen | ||||||||||||||||||||||||||||
| Full Title: Investigation of the influence of PAH-specific medication on right ventricular function in patients with pulmonary arterial hypertension (PAH) under basal conditions | ||||||||||||||||||||||||||||
| Medical condition: Pulmonary arterial Hypertension (PAH) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2012-003037-41 | Sponsor Protocol Number: MUG-EROS-2012 | Start Date*: 2012-09-21 | |||||||||||||||||||||
| Sponsor Name:Medizinische Universität Graz, Universitätsklinik für Innere Medizin, Klinische Abteilung für Lungenkrankheiten | |||||||||||||||||||||||
| Full Title: Effects of Roflumilast on pulmonary vascular resistance in patients with COPD and sleep apnea (Overlap Syndrome) with and without non-invasive ventilation. A Pilot Study. | |||||||||||||||||||||||
| Medical condition: This study is about pulmonary hypertension due to lung diseases. The lung disease in this study will be the overlap syndrome which is defined as chronic obstructive pulmonary disease concomitant wi... | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: AT (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| 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: 2016-004806-32 | Sponsor Protocol Number: RAMSES | Start Date*: 2019-03-02 | |||||||||||
| Sponsor Name:ITALIAN PULMONARY HYPERTENSION NETWORK, IPHNET | |||||||||||||
| Full Title: Right ventriculAr reverse reModeling and hemodynamic improvement after add-on combination therapy (ambriSentan/PDE-5i) in PAH patientS (RAMSES) | |||||||||||||
| Medical condition: patients with pulmonary arterial hypertention | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004971-42 | Sponsor Protocol Number: RVT-1201-2002 | Start Date*: 2021-10-26 | |||||||||||
| Sponsor Name:Altavant Sciences GmbH | |||||||||||||
| Full Title: A Phase 2b, Dose-Ranging, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Rodatristat Ethyl in Patients with Pulmonary Arterial Hypertension | |||||||||||||
| Medical condition: Pulmonary Arterial Hypertension (PAH) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) LV (Prematurely Ended) FR (Completed) BE (Completed) CZ (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) BG (Prematurely Ended) ES (Ongoing) AT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014246-29 | Sponsor Protocol Number: BPS-MR-PAH-203 | Start Date*: 2010-02-01 | |||||||||||
| Sponsor Name:Lung Rx | |||||||||||||
| Full Title: A 12-week, double-blind, international, multicenter, dose-response study of the safety and efficacy of Beraprost Sodium Modified Release (BPS-MR) in patients with pulmonary arterial hypertension (PAH) | |||||||||||||
| Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) BE (Prematurely Ended) DE (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003921-13 | Sponsor Protocol Number: 12/0368 | Start Date*: 2013-06-07 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: COMbination therapy for PulmonAry hypertension using RacEcadotril (COMPARE). | |||||||||||||
| Medical condition: Pulmonary hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-003725-22 | Sponsor Protocol Number: KKS-306 | Start Date*: 2023-04-20 | |||||||||||||||||||||
| Sponsor Name:Justus-Liebig-University Gießen | |||||||||||||||||||||||
| Full Title: Acute effect of iloprost (Ventavis®) inhalation in patients with exercise-induced pulmonary hypertension after a COVID-19 infection | |||||||||||||||||||||||
| Medical condition: Exercise-induced pulmonary hypertension after a COVID-19 infection | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2010-019883-36 | Sponsor Protocol Number: CAMN107X2201 | Start Date*: 2010-08-31 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A 24 week, randomized, double blind, multicenter, placebo-controlled efficacy, safety, tolerability and PK trial of Nilotinib (Tasigna®, AMN107) in Pulmonary Arterial Hypertension (PAH) | |||||||||||||
| Medical condition: Pulmonary Arterial Hypertension (PAH) Class II or III patients remaining symptomatic despite at least one PAH-specific therapy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) IT (Prematurely Ended) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-006787-25 | Sponsor Protocol Number: 16122021 | Start Date*: 2022-07-06 | |||||||||||||||||||||||||||||||
| Sponsor Name:Rigshospitalet The Heart Center | |||||||||||||||||||||||||||||||||
| Full Title: Effects of DAPAgliflozin on cardiopulmonary exercise capacity and hemodynamics in Pulmonary Arterial Hypertension: A double blind randomized trial | |||||||||||||||||||||||||||||||||
| Medical condition: Pulmonary arterial hypertension Chronic thromboembolic pulmonary hypertension | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| 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. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| 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: 2016-002389-29 | Sponsor Protocol Number: PULSE-COPD-007 | Start Date*: 2016-07-25 | ||||||||||||||||||||||||||
| Sponsor Name:Bellerophon Pulse Technologies, LLC | ||||||||||||||||||||||||||||
| Full Title: An Exploratory Clinical Study to Assess the Effect of Pulsed, Inhaled Nitric Oxide (iNO) on Functional Respiratory Imaging (FRI) Parameters in Subjects with World Health Organization (WHO) Group 3 ... | ||||||||||||||||||||||||||||
| Medical condition: Pulmonary Hypertension (PH) Associated with Chronic Obstructive Pulmonary Disease (COPD) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2007-003928-37 | Sponsor Protocol Number: BAY63-2521/12916 | Start Date*: 2008-07-14 | |||||||||||
| Sponsor Name:Bayer 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 patient... | |||||||||||||
| Medical condition: Patients with interstitial lung disease associated pulmonary hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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