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Aneurysm clinical trials

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NCT ID: NCT02528149 Completed - Clinical trials for Renal Artery Stenosis

Renal Arteries Dysplastic Aneurysms: Anatomopathological and Genetic Study

Start date: September 2013
Phase: N/A
Study type: Observational

Fibromuscular dysplasia (FMD) is localized structural defects in the arterial wall, whose innate or acquired character is still unknown. This segmental non atheromatous injury, leads to stenosis of the arteries of small and medium caliber. Renal arteries are the most commonly affected with 60-75% of total fibrodysplasia. Three histological subtypes have been described: intimal, medial and peri-medial. They are not mutually exclusive and can be observed in the same patient. This is a rare blood disease, occurring in children and young adults. In this young population with long life expectancy, these aneurysmal lesion are associated with 10% risk of rupture. To date, no data have shown in the literature that FMD is link to genetic causes, or if there is specific histopathologic lesions for non-atherosclerotic renal artery aneurysms. To answer these questions, Cardiovascular Surgery Unit of the University Hospital of Saint-Etienne, French national reference center for renal artery surgery, in association with the Reference Center for Rare Vascular Disease in Paris, designed the first study for pathological and genetic characteristics of dysplastic renal artery aneurysms in young patients.

NCT ID: NCT02507999 Completed - Cerebral Aneurysm Clinical Trials

Goal-directed Therapy in Endovascular Coiling of Cerebral Aneurysm Patients

Start date: November 2015
Phase: N/A
Study type: Interventional

Goal directed therapy (GDT) is a technique, which employs a non-invasive cardiac output monitoring (NICOM) device to guide management of circulating blood volume and blood pressure during procedures. The purpose of this study is to determine whether the use of goal-directed therapy to optimize blood volume and cardiac output during the procedure can improve the outcome of patients undergoing endovascular treatment of a brain aneurysm.

NCT ID: NCT02493296 Completed - Clinical trials for Abdominal Aortic Aneurysm

The Effect of Surgery on Central Aortic Pressure & haEmodynamics Study

ESCAPE
Start date: October 7, 2010
Phase:
Study type: Observational

The present study will investigate the effect of artificially stiffening the aorta by means of an aortic stent on central aortic haemodynamics (CAH). This study will determine whether aortic stenting inadvertently adversely impacts on CAH, thereby providing the rational for subsequent therapeutic intervention to reduce the associated cardiovascular risk.

NCT ID: NCT02487290 Completed - Clinical trials for Abdominal Aortic Aneurysm

ANEUFIX for Endoleaks Type II

ACP-T5
Start date: February 26, 2018
Phase: N/A
Study type: Interventional

The study is a non-randomized, multi-center safety and feasibility trial of Aneufix ACP-T5 to treat patients with Isolated type II endoleak in the presence of a non-shrinking AAA sac following an EVAR procedure.

NCT ID: NCT02479191 Completed - Clinical trials for Abdominal Aortic Aneurysm

LUCY Study: TriVascular Evaluation of Females Who Are Underrepresented Candidates for Abdominal Aortic Aneurysm Repair

LUCY
Start date: August 2015
Phase:
Study type: Observational [Patient Registry]

The LUCY Study is a prospective, consecutively enrolling, non-randomized multi center post-market registry to evaluate the low profile Ovation ® Abdominal Stent Graft Platform when used in the endovascular treatment of female patients.

NCT ID: NCT02477111 Completed - Clinical trials for Abdominal Aortic Aneurysms

European (EU) Post Approval Study of the INCRAFT® AAA Stent Graft System in Subjects With Abdominal Aortic Aneurysms

INSIGHT
Start date: March 30, 2015
Phase:
Study type: Observational

INSIGHT is a postmarket clinical follow-up study in the European Union. The purpose of the study is to continue to evaluate the safety and effectiveness/performance of INCRAFT in subjects with abdominal aortic aneurysms requiring endovascular repair in routine clinical practice. Approximately 150 subjects will be enrolled and followed through 5-years post procedure. Up to 25 sites in Europe may participate.

NCT ID: NCT02467062 Completed - Clinical trials for Aortic Valve Disease

Implementation of Non-size Markers Derived From 4D Flow MRI of Patients With Aortic Disease.

Start date: September 2015
Phase: N/A
Study type: Interventional

The aim of the investigator is to implement 4D FLOW MRI technique into a clinical setting and evaluate the blood flow pattern and wall sheer stress in patients with aortic and/or aortic valve diseases.

NCT ID: NCT02465125 Completed - Anemia Clinical Trials

The Transfusion Triggers in Vascular Surgery Trial

TV
Start date: July 15, 2015
Phase: Phase 2
Study type: Interventional

BACKGROUND - Vascular surgical patients often receive red blood cell (RBC) transfusions in the peri-operative period - RBC transfusion may lead to improved outcome but on the other hand the intervention may be harmful - Danish Health and Medicines Authority recommends transfusion of RBC at hemoglobin below 5 mmol/L while local clinical guidelines recommend transfusion of RBC to maintain hemoglobin levels above 6 mmol/L - A large randomized clinical trial is needed to evaluate the efficacy and safety of RBC transfusion in patients undergoing vascular surgery. - A trial examining the effect of RBC transfusion on tissue oxygenation is used to test the trial-design and feasibility for a trial evaluating post-operative mortality and morbidity.

NCT ID: NCT02463760 Completed - Clinical trials for Aortic Aneurysm, Abdominal

Predicting Rupture of AAA by Anatomic and Hemodynamic Markers

Start date: August 2015
Phase:
Study type: Observational

The purpose of the study is to investigate imaging findings, which can help us to predict factors contributing to abdominal aortic aneurysm growth and rupture.

NCT ID: NCT02462876 Completed - Clinical trials for Popliteal Artery Aneurysm

Evaluation of the GORE® VIABAHN® Endoprosthesis for the Treatment of Popliteal Artery Aneurysm (PAA)

Start date: October 2015
Phase:
Study type: Observational

This study will assess the long term safety and performance of the GORE® VIABAHN® Endoprosthesis for the treatment of patients with Popliteal Artery Aneurysms.