- Trials with a EudraCT protocol (17)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
17 result(s) found for: Thoracic aorta.
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EudraCT Number: 2022-000513-14 | Sponsor Protocol Number: NBK154/2/2021 | Start Date*: 2023-03-08 |
Sponsor Name:Medical University of Gdańsk | ||
Full Title: Evaluation of the Efficacy of Valsartan in Slowing Down Aortic Root Dilatation in Children and Young Adults with Marfan-type Heritable Thoracic Aortic Diseases – Valsar-TAD, a randomised, double-b... | ||
Medical condition: Marfan Syndrome Diseases related to Marfan syndrome (rare diseases with aneurysms of the thoracic aorta and dissection of the aorta), among others: Loeys-Dietz syndrome, Vascular type of Ehlers-Da... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: PL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000538-12 | Sponsor Protocol Number: HLK-VASC-11/01 | Start Date*: 2011-06-14 |
Sponsor Name:VU University Medical Center | ||
Full Title: An exploratory open-label PET-observer-blinded pilot study to evaluate the effect of 3 and 12 months treatment with Aliskeren-based versus amlodipin-based antihypertensive treatment in patients wit... | ||
Medical condition: Abdominal Aortic Aneurysm Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002820-18 | Sponsor Protocol Number: NL45370.020.13 | Start Date*: 2014-07-11 |
Sponsor Name:St. Antonius Hospital | ||
Full Title: Comparison of a single dose fibrinogen with placebo and the number of blood transfusions after ascending aorta surgery (FIBTEG study) | ||
Medical condition: Patients who need thoracic aortic reconstruction surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018767-42 | Sponsor Protocol Number: CEUS-TEVAR-29 | Start Date*: 2011-05-06 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: The use of Contrast Enhanced Transesophageal Echocardiography in thoracic endovascular aortic repair (TEVAR). Feasibility and safety of a new tool for intraoperative monitoring and follow up. | |||||||||||||
Medical condition: descending thoracic aorta diseases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000452-28 | Sponsor Protocol Number: VIPER-OCTA | Start Date*: 2014-11-05 | |||||||||||
Sponsor Name:Section for Transfusion Medicine, Capitol Region Blood Bank | |||||||||||||
Full Title: Vasculopathic Injury and Plasma as Endothelial Rescue – OCTAplas trial | |||||||||||||
Medical condition: patients undergoing emergency surgery for thoracic aortic dissections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004612-31 | Sponsor Protocol Number: BI3023_2002 | Start Date*: 2008-05-29 | |||||||||||
Sponsor Name:CSL Behring GmbH | |||||||||||||
Full Title: Efficacy and safety of Haemocomplettan® P in patients experiencing acute bleeding while undergoing aortic replacement surgery | |||||||||||||
Medical condition: Acute bleeding while undergoing aortic replacement surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003998-28 | Sponsor Protocol Number: CER-001-CLIN-003 | Start Date*: 2012-01-24 | |||||||||||
Sponsor Name:Cerenis Therapeutics | |||||||||||||
Full Title: Modifying Orphan Disease Evaluation (MODE) Study: A Multicenter, Open-Label Study of the Effects of CER-001 on Plaque Volume in Subjects with Homozygous Familial Hypercholesterolemia (HoFH) | |||||||||||||
Medical condition: homozygous familial hypercholesterolemia | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001447-31 | Sponsor Protocol Number: 954 | Start Date*: 2014-01-14 |
Sponsor Name:Liverpool Heart and Chest Hospital NHS Foundation Trust | ||
Full Title: A randomised controlled trial to study the effect of acetazolamide on the incidence of blood-stained CSF, effect on cerebrospinal fluid (CSF) pressure, CSF drainage and neurological dysfunction in ... | ||
Medical condition: Elevated cerebrospinal fluid pressure in patients undergoing thoracic-abdominal aortic repair | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003088-76 | Sponsor Protocol Number: 11-170 | Start Date*: 2014-07-14 |
Sponsor Name:Clinical Evaluation Research Unit (CERU) | ||
Full Title: SodiUm SeleniTe Adminstration IN Cardiac Surgery surgery (SUSTAIN CSX®-trial) - A randomized controlled trial of high dose sodium-selenite administration in high risk cardiac surgical patients | ||
Medical condition: Selenium is a key component of a number of selenoproteins which protect against oxidative stress and is well recognised for its prominent role in immune defence. Selenoproteins have the potential t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000236-26 | Sponsor Protocol Number: CRLX030X2201 | Start Date*: 2012-11-06 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An exploratory study to investigate the haemodynamic effects of serelaxin in patients with compensated cirrhosis and portal hypertension | |||||||||||||
Medical condition: Compensated alcohol-related cirrhosis and portal hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000752-20 | Sponsor Protocol Number: PETSPA | Start Date*: 2015-06-29 | |||||||||||
Sponsor Name:University of Helsinki | |||||||||||||
Full Title: The efficacy of adalimumab and conventional antirheumatic drugs in alleviating axial and aortic inflammation detected in PET/CT in patients with axial spondyloarthritis | |||||||||||||
Medical condition: Axial and aortic inflammation detected in PET/CT imaging in patients with axial spondyloarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002834-59 | Sponsor Protocol Number: SNFCT2015-05 | Start Date*: 2016-11-28 | |||||||||||||||||||||
Sponsor Name:Sanifit Therapeutics S.A. | |||||||||||||||||||||||
Full Title: A double-blind, randomised, placebo-controlled study to assess the effect of SNF472 on progression of cardiovascular calcification on top of standard of care in end-stage-renal-disease (ESRD) patie... | |||||||||||||||||||||||
Medical condition: Cardiovascular calcification in blood vessels in end-stage-renal-disease (ESRD) patients on haemodialysis (HD). | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) ES (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-003000-32 | Sponsor Protocol Number: ACTRN12619001355167 | Start Date*: 2023-06-23 | |||||||||||||||||||||
Sponsor Name:Monash University | |||||||||||||||||||||||
Full Title: 20% Albumin infusion and AKI following cardiac surgery – Randomised Trial | |||||||||||||||||||||||
Medical condition: Acute kidney injury (AKI) is a common complication of cardiac surgery. AKI is defined according to KDIGO criteria in 3 severity stages. KDIGO creatinine-based criteria for diagnosis and staging of... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003731-35 | Sponsor Protocol Number: 20130293 | Start Date*: 2016-02-26 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized Double-blind Placebo Controlled Study Characterizing The Effects of PCSK9 Inhibition On Arterial Wall inflammation in Patients With Elevated Lp(a) | |||||||||||||
Medical condition: Hypercholesterolemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005655-16 | Sponsor Protocol Number: Regard-CrC_2012 | Start Date*: 2013-07-03 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: Regorafenib Assessment in Refractory advanced Colorectal cancer | |||||||||||||
Medical condition: Advanced refractory colorectal cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006174-47 | Sponsor Protocol Number: FC-004 | Start Date*: 2012-06-08 | |||||||||||
Sponsor Name:ProFibrix BV | |||||||||||||
Full Title: A Phase 3, Randomized, Single-Blind, Controlled Trial of Topical Fibrocaps™ in Intraoperative Surgical Haemostasis | |||||||||||||
Medical condition: Intraoperative Surgical Hemostasis (Spinal Surgery, Vascular Surgery, Hepatic resection, Soft tissue dissection) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) GB (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2012-004860-22 | Sponsor Protocol Number: IJB-BCTL:20120306 | Start Date*: 2014-01-16 | |||||||||||
Sponsor Name:Institute Jules Bordet | |||||||||||||
Full Title: The [PEARL] Study : Pet imaging as a biomarker of Everolimus Added value in hormone Refractory postmenopausaL women | |||||||||||||
Medical condition: Locally advanced or metastatic endocrine receptor positive and HER2 negative breast cancer refractory to non-steroidal aromatase inhibitors (NSAI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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