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Aneurysm clinical trials

View clinical trials related to Aneurysm.

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NCT ID: NCT02949297 Completed - Clinical trials for Aortic Aneurysm, Abdominal

Expanding Patient Applicability With Polymer Sealing Ovation Alto Stent Graft Investigational Device Exemption (IDE) Study

ELEVATE
Start date: March 30, 2017
Phase: N/A
Study type: Interventional

A prospective clinical evaluation of the effectiveness of the Ovation Alto Abdominal Stent Graft System when used in the treatment of subjects with abdominal aortic aneurysm (AAA).

NCT ID: NCT02934087 Completed - Clinical trials for Abdominal Aortic Aneurysm (AAA)

Endovascular Aneurysm Repair (EVAR) Gate Study

EVAR
Start date: August 2011
Phase: N/A
Study type: Interventional

This study will evaluate a randomized comparison of direct versus snare techniques for cannulation of contralateral gate during an endovascular aneurysm repair (EVAR) procedure. This information will be used to determine if primary snaring is superior to retrograde cannulation in decreasing procedural time and radiation exposure.

NCT ID: NCT02921711 Completed - Clinical trials for Intracranial Aneurysms

TRAIL: Treatment of Intracranial Aneurysms With LVIS® System

TRAIL
Start date: June 2012
Phase:
Study type: Observational [Patient Registry]

A prospective, multicenter, observational assessment of the safety and effectiveness of the LVIS® device in the treatment of wide necked intracranial aneurysms.

NCT ID: NCT02921698 Completed - Clinical trials for Intracranial Aneurysms

Safety and Efficacy Analysis of FRED® Embolic Device in Aneurysm Treatment

SAFE
Start date: July 2014
Phase:
Study type: Observational [Patient Registry]

A prospective, multicenter, observational evaluation of the safety and efficacy of the FRED® device in the treatment of intracranial aneurysms.

NCT ID: NCT02907229 Completed - Clinical trials for Intracranial Aneurysm

Safety and Efficacy of Honeycomb Microporous Covered Stents (NCVC-CS1) for the Treatment of Intracranial Aneurysms

NCVC-CS1_UAN
Start date: May 2016
Phase: N/A
Study type: Interventional

This trial is conducted to evaluate the safety and technical effectiveness of using NCVC-CS1, a newly developed honeycomb microporous covered stent, for the treatment of intracranial aneurysms which are difficult to be cured by conventional surgical or endovascular procedures.

NCT ID: NCT02881957 Completed - Stroke Clinical Trials

Hypovitaminosis D in Neurocritical Patients

Start date: October 10, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Vitamin D has been shown to impact prognosis in a variety of retrospective and randomized clinical trials within an intensive care unit (ICU) environment. Despite these findings, there have been no studies examining the impact of hypovitaminosis D in specialized neurocritical care units (NCCU). Given the often significant differences in the management of patients in NCCU and more generalized intensive care units there is a need for further inquiries into the impact of low vitamin D levels in this specific environment. This study proposes a randomized, double-blinded, placebo-controlled, single center evaluation of vitamin D supplementation in the emergent NCCU patient population. The primary outcome will involve length-of-stay for emergent neurocritical care patients. Various secondary outcomes, including in-hospital mortality, ICU length-of-stay, Glasgow Outcome Score on discharge, complications and quality-of-life metrics. Patients will be followed for 6 months post-discharge.

NCT ID: NCT02876263 Completed - Clinical trials for Coronary Artery Disease

Noninvasive Neuromonitoring of Surgery of the Thoracic Aorta

Start date: September 2007
Phase: N/A
Study type: Observational

The aim of this prospective, explorative study of noninvasive neuromonitoring was to search potential and practical methods associated with neurological outcome in the perioperative and immediate postoperative setting of surgery of the thoracic aorta. These methods include abbreviated EEG monitoring, near-infrared spectroscopy, transcranial Doppler ultrasound and biochemical markers associated with neuronal damage.

NCT ID: NCT02875444 Completed - Clinical trials for Abdominal Aortic Aneurysm

Measurement of Maximum Diameter of Native Abdominal Aortic Aneurysm by Angio-CT

AAA-angioCT
Start date: January 2013
Phase: N/A
Study type: Observational

Screening for an abdominal aortic aneurysm, monitoring its growth and evaluation of its risk of rupture are based on the measure of its maximum diameter. The abdominal aortic aneurysm's treatment to prevent its rupture is recommended from a threshold of 50-55 mm in men and of 45-50 mm in women. The importance of this measure for patient management justify a specific and homogeneous protocol of measure. However, the diversity of methods of measuring the maximum diameter with scanner and ultrasound was shown. The impact of various angio-CT based measures of maximum AAA diameter, and the impact of reproducibility limits on the decision to operate have never been investigated.

NCT ID: NCT02867501 Completed - Vascular Diseases Clinical Trials

Venous Distension in Patients With Aneurysmatic Arterial Disease

Start date: May 2016
Phase: N/A
Study type: Observational

The aim of the study is to assess if venous distension in patients with aneurysmatic arteriopathy is higher compared to patients with peripheral arterial occlusive disease (PAOD) and in controls.

NCT ID: NCT02866812 Completed - Clinical trials for Intracranial Aneurysm

Prevalence and Factors Associated With the Occurrence of Depression Six Months After an Endovascular Treatment of Intracranial Aneurysm

DEP-AIC
Start date: March 17, 2016
Phase: N/A
Study type: Interventional

During the last decade, the embolization has become the treatment of choice for ruptured intracranial aneurysms, to improve the neurological outcome of patients. At the same time, for his safety, she also became the technique allowing prophylactic treatment of unruptured intracranial aneurysms discovered incidentally during imaging exams. Regarding patients with ruptured intracranial aneurysms, patients who survive often have a reduced quality of life while one in two has a good neurological outcome after embolization. Depression, anxiety and fatigue, whose the psycho-social impact is important, are often cited. This description has often been done without considering the realized type of treatment (surgery or embolization) and mostly of neurological and functional status of the patient remotely (disability or not in daily activities). Regarding patients with unruptured intracranial aneurysms, they are mostly asymptomatic and embolization is programmed. They would present an cognitive impairment in one case in five at 1 month of treatment. If depression, fatigue and difficult return to working life are logically found in patients with severe sequelae (disability in daily activities) of their ruptured intracranial aneurysms, the question arises for patients with a ruptured intracranial aneurysms with a favorable evolution and for asymptomatic patients with unruptured intracranial aneurysms. A precise status of these populations is necessary, especially as the discovery and treatment of their intracranial aneurysms is often early (between 40 and 60 years) and that their good neurological status should allow "a priori" to return easily at the active life.