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Aortic Aneurysm, Abdominal clinical trials

View clinical trials related to Aortic Aneurysm, Abdominal.

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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: NCT01526811 Completed - Clinical trials for Cardiovascular Diseases

Endurantâ„¢ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic Aneurysms (ENDURANT France)

Start date: March 2012
Phase:
Study type: Observational

The purpose of this study is to assess the benefits of endovascular repair with Endurant Stent Graft System by documenting overall mortality, complications, the rate of conversion to open surgical repair, and the development and rupture of the aneurysm on a long term, i.e. at 5 years, in a cohort of patients representative of the population treated under real-life conditions of use in France.

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: NCT01491945 Completed - Clinical trials for Abdominal Aortic Aneurysm

Safety and Effectiveness Trial of the Ventana Fenestrated Stent Graft System

Start date: March 3, 2013
Phase: N/A
Study type: Interventional

The purpose of this trial is to determine if the Ventana Fenestrated Stent Graft System is safe and effective for the endovascular repair of juxtarenal or pararenal aortic aneurysms.

NCT ID: NCT01480206 Completed - Carotid Stenosis Clinical Trials

Overlay of 3D Scans on Live Fluoroscopy for Endovascular Procedures in the Hybrid OR

Start date: September 13, 2011
Phase:
Study type: Observational

As endovascular procedures become more complex, there is a growing need for 3D image overlay to assist with device guidance and placement. Currently, a 3D image is typically created intra-operatively using 3D rotational angiography (3D-RA) or cone-beam CT (XperCT). This 3D image may then be overlaid on live fluoroscopy to provide 3D guidance information (Dynamic 3D Roadmapping). Philips Healthcare multimodality overlay products allows registration of a pre-acquired MR/CT or 3D rotational image to live fluoroscopy.

NCT ID: NCT01465425 Enrolling by invitation - Clinical trials for Pancreatic Neoplasms

Extracolonic Findings on Computed Tomography (CT) Colonography

ACRIN7151
Start date: September 2011
Phase:
Study type: Observational

The ACRIN 7151 trial will use medical records abstraction data from participants with extracolonic findings (ECFs) reported from the ACRIN 6664 National CT Colonography Trial to: 1) measure incidence of diagnostic imaging, hospitalization, and interventional procedures associated with ECFs reported on computed tomography colonography (CTC), delineated by type of ECF; 2) determine potential predictors of follow-up diagnostic imaging, hospitalization, and interventional procedures, delineated by type of ECF; and 3) evaluate the clinical/pathologic diagnoses associated with indeterminate but potentially significant ECFs. These data can be used to incorporate ECFs into existing models on the cost-effectiveness of CTC in colorectal cancer screening and can potentially be used to develop guidelines for the reporting and management of ECFs.

NCT ID: NCT01452620 Completed - Clinical trials for Endovascular Abdominal Aortic Aneurysm Repair (EVAR)

Endovascular Abdominal Aortic Aneurysm Repair by Interventional Cardiologists

EVAR
Start date: January 2011
Phase: N/A
Study type: Observational

Registry for Endovascular repair of abdominal aortic aneurysm performed primarily by Interventional Cardiologists

NCT ID: NCT01450501 Active, not recruiting - Clinical trials for Aortic Aneurysm, Abdominal

Chronic Q-fever in Patients With an Abdominal Aortic Disease (QAAD-study)

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

Q-fever is a zoonosis caused by Coxiella burnetii, an intracellular bacterium. Since the epidemic outbreak of acute Q-fever in Holland nearly 4030 people have been registered with the acute form of the disease. Knowing that only 40% of all infected people develop symptoms, the number of infected people (and potential candidates for chronic Q-fever) are much higher. Chronic Q-fever generally manifest itself after a couple of months or years after the primary infection (in 1-5% of all cases). The clinical presentation can be a life-threatening and frequently underdiagnosed disease, as endocarditis, infected aneurysm and vascular prosthesis or chronic Q-fever related to pregnancy and immunecompromised patients. That's why a screening program is started in the endemic area and trace patients with chronic Q-fever. So eventually, a greater group of patients with chronic vascular Q-fever can be described. In addition, there is still no therapeutic guideline for management of chronic Q-fever in patient with a vascular chronic Q-fever. Patients with an aneurysm or vascular graft will be screened for chronic Q-fever. Patients with chronic Q-fever will be included in a follow-up program, in which additional research and treatment will start. The initial treatment of patients with chronic Q-fever is doxycycline and hydroxychloroquine for at least 18 months. In addition, patients will be monitored in 3-monthly controls, blood samples and imaging will be done. Parameters as complaints, titers, circulating DNA, grow of aneurysm, complications etc. will be investigated. Ultimately, the current therapeutic guideline for management of C. burnetii will be evaluated if it can also be applied for patients with vascular chronic Q-fever.

NCT ID: NCT01425242 Terminated - Hypertension Clinical Trials

Study on Anti-inflammatory Effect of Anti-hypertensive Treatment in Patients With Small AAA's and Mild Hypertension

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

Inflammation of the blood vessel plays an important role in the development and growth of a dilated abdominal aorta. An elevated blood pressure leads to an increase in inflammation, therefore blood pressure lowering is an important part of the treatment of patients with a dilated abdominal aorta who also have an elevated blood pressure. In the investigators study the investigators compare the anti-inflammatory effects of 2 different blood pressure lowering strategies. The investigators hypothesize that both strategies will decrease inflammation, however the investigators believe the total decrease of inflammation depends on the type of blood pressure lowering medication used.

NCT ID: NCT01424267 Terminated - Clinical trials for Abdominal Aortic Aneurysm

Zenith® LP Abdominal Aortic Aneurysm (AAA) Post-Market Registry

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

A registry to collect additional prospective intra-operative and follow-up information on physician use of the CE-marked Zenith® Low Profile Abdominal Aortic Aneurysm (AAA) Endovascular Graft under routine clinical care.