- Trials with a EudraCT protocol (267)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
267 result(s) found for: Pulmonary Arterial Hypertension.
Displaying page 1 of 14.
EudraCT Number: 2009-014534-15 | Sponsor Protocol Number: NACIPP | Start Date*: 2009-10-01 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: EFFECT OF ACUTE ADMINISTRATION OF N-ACETYLCYSTEINE ON BLOOD PRESSURE OF PULMONARY ARTERIAL IN PRIMARY PULMONARY HYPERTENSION. | |||||||||||||
Medical condition: PRIMARY PULMONARY HYPERTENSION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003847-37 | Sponsor Protocol Number: REM 04 15 | Start Date*: 2004-12-21 | |||||||||||
Sponsor Name:BIOPROJET | |||||||||||||
Full Title: An Open label uncontrolled study of the safety and efficacy of chronic intravenous Remodulin in patients with pulmonary Arterial Hypertension | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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 (Restarted) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000347-14 | Sponsor Protocol Number: PROCLAIM | Start Date*: 2016-06-16 | ||||||||||||||||
Sponsor Name:IDIBAPS | ||||||||||||||||||
Full Title: Cell proliferation in pulmonary hypertension: mollecular imaging detection by FDG PET. Comparative study between patients and healthy subjects | ||||||||||||||||||
Medical condition: Pulmonary artery hypertension and thromboembolic chronic pulmonary hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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: 2007-003975-38 | Sponsor Protocol Number: TERPAH-001 | Start Date*: 2007-11-22 | |||||||||||
Sponsor Name:Ergonex Pharma GmbH | |||||||||||||
Full Title: Proof of Concept Study to Investigate the Efficacy, Haemodynamics and Tolerability of Terguride vs. Placebo in Patients with Pulmonary Arterial Hypertension. Double-blind, randomized, prospective P... | |||||||||||||
Medical condition: Pulmonary arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) NL (Completed) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004224-37 | Sponsor Protocol Number: EREMIT | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Universität Leipzig | |||||||||||||
Full Title: Everolimus in der Therapie von Patienten mit pulmonaler Hypertonie | |||||||||||||
Medical condition: - steady or progressive pulmonary hypertension accompanied by at least two of the following parameters associated with a poor prognosis: - Cardiac index ≤ 2,1 l/min/m2 - 6 MWD ≤ 380 m - systolic RR... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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: 2007-001643-21 | Sponsor Protocol Number: 2007OE002B | Start Date*: 2008-06-26 | |||||||||||
Sponsor Name:Royal Brompton and Harefield NHS Trust | |||||||||||||
Full Title: Use of endothelin-1 antagonists in patients with Established Pulmonary Hypertension and Fibrotic Lung Disease. – A randomised, placebo-controlled, double-blinded study. | |||||||||||||
Medical condition: Pulmonary hypertension in patients with interstitial lung disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006453-12 | Sponsor Protocol Number: NS-304/-03 | Start Date*: 2008-07-21 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | |||||||||||||
Full Title: A multi-centre, multinational, open- label study to evaluate the long-term safety, tolerability and efficacy of selexipag / ACT-293987 (NS-304) in the treatment of pulmonary arterial hypertension i... | |||||||||||||
Medical condition: Pulmonary arterial hypertension (PAH) (idiopathic PAH, familial PAH, and PAH associated with collagen disease, corrected congenital vitium or anorexigen use | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) AT (Completed) FR (Completed) BE (Completed) GB (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001675-37 | Sponsor Protocol Number: Lis-Safe | Start Date*: 2012-07-24 | |||||||||||
Sponsor Name:Sinoxa Pharma GmbH | |||||||||||||
Full Title: A Prospective, Open-label, Exploratory Study to Investigate the Safety, Efficacy, and Haemodynamics of Lisuride Subcutaneous Infusion as Add-on to Conventional Treatment in Patients with Pulmonary ... | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003694-27 | Sponsor Protocol Number: AC-055-303 | Start Date*: 2011-11-17 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | |||||||||||||
Full Title: SERAPHIN-OL: Study with an ERA in Pulmonary arterial Hypertension to Improve cliNical outcome (Open Label) Long-term single-arm open-label extension study of the SERAPHIN study, to assess the safe... | |||||||||||||
Medical condition: symptomatic pulmonary arterial hypertension | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) NL (Completed) FR (Completed) FI (Prematurely Ended) SE (Completed) AT (Completed) BE (Completed) DK (Completed) SK (Completed) PT (Prematurely Ended) IT (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001893-24 | Sponsor Protocol Number: Bay63-2521/14986 | Start Date*: 2011-10-13 | |||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||||||||||||
Full Title: Relative bioavailability and food effect study of two oral liquid formulations in comparison to a 1mg tablet of riociguat to characterize its pharmacokinetic properties in healthy male and female a... | |||||||||||||||||||||||
Medical condition: Children with PH due to • Pulmonary arterial hypertension (PAH) • persistent pulmonary hypertension of the newborn (PPHN) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
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: 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: 2007-001645-17 | Sponsor Protocol Number: 2007OE003B | Start Date*: 2007-12-04 | |||||||||||
Sponsor Name:Royal Brompton and Harefield NHS Trust | |||||||||||||
Full Title: Prevention of Established Pulmonary Hypertension in High Risk patients with Fibrotic Lung Disease – a double-blinded, randomised, placebo controlled trial with endothelin-1 receptor antagonist the... | |||||||||||||
Medical condition: Pulmonary hypertension in patients with interstitial lung disease. Specifically this trial looks at patients who have mild pulmonary hypertension, or are in an at-risk group to developing pulmonar... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018436-41 | Sponsor Protocol Number: Bay 63-2521/14554 | Start Date*: 2010-05-11 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Acute hemoDynamic effects of RIociguat (BAY 63-2521) in patients with puLmonary hypertension Associated with diasTolic heart failurE (DILATE 1): A randomized, double-blind, placebo-controlled, sin... | |||||||||||||
Medical condition: Pulmonary hypertension associated with diastolic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) CZ (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003621-24 | Sponsor Protocol Number: MG-101-01 | Start Date*: 2008-05-29 | ||||||||||||||||||||||||||
Sponsor Name:MondoGEN AG | ||||||||||||||||||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, dose-finding, parallel-group study to assess the hemodynamic effects, clinical efficacy, tolerability and safety of Aviptadil (Vasoactive Intestinal Pe... | ||||||||||||||||||||||||||||
Medical condition: Pulmonary arterial hypertension (PAH) due to idiopathic pulmonary arterial hypertension (IPAH), familial PAH or PAH associated with connective tissue diseases (CTD) (e.g. systemic sclerosis, system... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) BE (Completed) NL (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) DE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003328-39 | Sponsor Protocol Number: NS-304/-02 | Start Date*: 2008-04-25 | ||||||||||||||||||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | ||||||||||||||||||||||||||||
Full Title: A multi-centre, multinational, open-label single-dose acute hemodynamic study followed by a multi-centre, multinational, randomized, double-blind, parallel-group, placebo controlled study to assess... | ||||||||||||||||||||||||||||
Medical condition: pulmonary arterial hypertension (PAH) (idiopathic PAH, familial PAH, and PAH associated with collagen disease, corrected congenital vitium or anorexigen use) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) DE (Completed) HU (Completed) AT (Completed) GB (Completed) IT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002783-12 | Sponsor Protocol Number: BAYq6256/16483 | Start Date*: 2014-01-07 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A multi-center, open-label, randomized cross-over study to compare the acute tolerability and pharmacokinetics of BAY Q 6256 (iloprost; Ventavis) inhalation using the I-Neb nebulizer and the FOX ne... | |||||||||||||
Medical condition: Patients with Pulmonary arterial hypertension, WHO class III, who have been on therpay with Ventavis 10 for at least 4 weeks | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
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