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Aortic Aneurysm clinical trials

View clinical trials related to Aortic Aneurysm.

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NCT ID: NCT01538056 Recruiting - Clinical trials for Abdominal Aortic Aneurysms

Physician Modified Endovascular Grafts

PMEG
Start date: March 2011
Phase: N/A
Study type: Interventional

The primary objectives of this study are to determine whether physician modified endovascular grafts are a safe and effective method of treating patients with elective, symptomatic or ruptured juxtarenal aortic aneurysms in those patients considered to be unsuitable candidates for open surgical repair and have no other options for treatment.

NCT ID: NCT01524211 Recruiting - Clinical trials for Thoracoabdominal Aortic Aneurysm

Evaluation of Branch Endografts in the Treatment of Aortic Aneurysms

Start date: January 25, 2012
Phase: N/A
Study type: Interventional

Zenith t-Branch Study Cohort: The purpose of this study is to collect information on the Cook Zenith t-Branch endovascular stent-graft system and the Terumo Arch Branch for the treatment of aortic aneurysms. Terumo Arch Branch Study Cohort: The purpose of this additional study arm to the current IDE clinical trial is to collect a priori information on the Terumo Arch Branch Endograft for the treatment of proximal thoracic aortic pathologies that cannot be treated with conventional thoracic endografts.

NCT ID: NCT01523262 Recruiting - Aortic Aneurysm Clinical Trials

Preventing Myocardial Ischemia by Preconditioning in Elective Operation for Abdominal Aortic Aneurysm

Start date: January 2011
Phase: Phase 1
Study type: Interventional

Primary To investigate whether peripheral predonditioning induced by brief, intermittent constriction of blood supply to an arm can reduce the incidence of perioperative myocardial ischemia in patients operated electively for infrarenal aortic aneurysm. Secondary To investigate the impact of peripheral preconditioning on perioperative inflammatory response. To investigate whether peripheral preconditoning can protect against perioperative myocardial infarction and reduced cardiac pump function.

NCT ID: NCT01505309 Recruiting - Aorta Aneurysm Clinical Trials

Endovascular Aortic Repair for Aortic Dissection

Start date: January 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the short to mid term efficacy and safety of Thoracic Endovascular Aortic Repair (TEVAR) in patients who had aortic lesions, such as descending aortic/arch aneurysm, pseudo-aneurysm, Stanford Type B dissection, dissection with primary tear located in the aortic arch, et al.

NCT ID: NCT01500395 Recruiting - Aorta Aneurysm Clinical Trials

Hybrid Operation in Thoracic Aortic Dissection

Start date: November 2011
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to investigate the short to mid term efficacy and safety of different hybrid operations who had complex aortic lesions, such as ascending aortic/arch aneurysm, pseudo-aneurysm, Stanford Type A dissection, retrograde Stanford Type B dissection, dissection with primary tear located in the aortic arch, et al.

NCT ID: NCT01496833 Recruiting - Aorta Aneurysm Clinical Trials

Total Endovascular Aortic Arch Re-construction Study(TEARS)

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

The purpose of this study is to investigate the short to mid term efficacy and safety of a newly-developed branched stent graft in patients who had complex aortic lesions, such as ascending aortic/arch aneurysm, pseudo-aneurysm, Stanford Type A dissection, retrograde Stanford Type B dissection, dissection with primary tear located in the aortic arch, et al.

NCT ID: NCT01390181 Recruiting - Clinical trials for Thoracic Aortic Aneurysm

The Effect of Losartan in Bicuspid Aortic Valve Patients

Start date: September 2011
Phase: N/A
Study type: Interventional

The specific aims of this study are to: - Establish baseline levels of circulating MMP-2 and -9 , TIMP-1and- 2 and TGFB levels in individuals with bicuspid aortic valve and ascending aortic or aortic sinus measurements >40mm. - Assess the effect on MMP levels during treatment with losartan, an angiotensin II receptor blocking agent. - In the setting of losartan therapy for one year, evaluate the response of MMP levels in these patients, and clinical outcomes including effects on aortic growth rate

NCT ID: NCT01306734 Recruiting - Clinical trials for Ascending Aorta Aneurism

Hypothermia and Circulatory Arrest During Surgery on the Ascending Aorta: A Comparison Between Two Cooling Methods

Start date: March 2011
Phase: N/A
Study type: Observational

PURPOSE: To compare crash cooling versus gradient cooling methods for patients undergoing planned surgery on the ascending aorta in deep hypothermic circulatory arrest. To investigate the impact of hypothermia and circulatory arrest on the coagulation, stress-response, and cerebral outcome. BACKGROUND: Cooling to 18 °C using extracorporeal circulation allows for circulatory arrest during surgery on the ascending aorta. Two different methods are used either lowering the temperature of the blood by 10 °C at a time, gradient cooling, or as cold as possible, crash cooling. The distribution of hypothermia is expected to be different for the two methods, the latter predominantly cooling the body core. The influence on the physiological response is expected to vary with the two methods. The surgical procedure and the cooling greatly elicit a stress response and the coagulation is profoundly influenced. There can be adverse effects on the neurological outcome due to the procedure. The two methods are considered equal, but have never been subjected to comparison. The surgery and circulatory changes can have a negative influence on the cerebral outcome . METHODS: Twenty patients between 18 and 80 yrs randomized either to crash cooling or gradient cooling, ten patients in each group.. Patients with severe comorbidities or known coagulopathy are excluded. Anesthesia and operation as performed routinely in the department. The primary endpoint is duration of cooling, secondary endpoints include coagulation parameters (thromboelastography, clot stability), stress response parameters (adhesion molecule expression on endothelial cells, oxidative stress analysis, inflammatory markers), neuropsychological tests, MRI of the cerebrum, markers of cerebral ischemia, and ultrasound imaging of the great vessels for detection of air bubbles. Baseline values are obtained for all parameters.

NCT ID: NCT01291290 Recruiting - Clinical trials for Ruptured Abdominal Aortic Aneurism

START - Early Thrombocyte Administration to Patients With Ruptured Abdominal Aortic Aneurism

rAAA
Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of platelet infusion prior to transfer to a vascular surgical department in patients with a ruptured abdominal aortic aneurism.

NCT ID: NCT01205945 Recruiting - Clinical trials for Aortic Aneurysm, Abdominal

The Effect of Abdominal Aortic Aneurysm Screening on Mortality in Asian Population

Start date: August 2010
Phase: N/A
Study type: Observational

Abdominal aortic aneurysm(AAA) occurs when the infrarenal aorta expands to a maximal diameter of 3.0cm or greater. Although AAA may asymptomatic for many years, almost one third eventually rupture if left untreated. Several randomized trials showed that ultrasonographic screening for AAA could reduce the frequency of acute operations and AAA-related mortality. However, all of randomized trials were performed in Western countries. There was no randomized trials for AAA screening in Asian countries. This randomized, controlled trial is to analyze the benefits of screening old population for AAA in Korea.