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Aortic Aneurysm clinical trials

View clinical trials related to Aortic Aneurysm.

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NCT ID: NCT01055275 Terminated - Aortic Aneurysm Clinical Trials

Cook Iliac Branch Graft Post-market Registry

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

The Cook Iliac Branch Graft Post-market Registry will obtain case reports of physician experience with a CE-marked Cook Iliac Branch Graft to further confirm device safety and performance.

NCT ID: NCT01033370 Terminated - Aortic Aneurysm Clinical Trials

A Safety and Efficacy Study of Blood Pressure Control in Acute Aortic Emergencies - A Pilot Study (PROMPT)

PROMPT
Start date: November 2009
Phase: Phase 4
Study type: Interventional

This study is a single center, non-randomized, open-label, pilot efficacy and safety study evaluating the ability of clevidipine IV antihypertensive to rapidly control elevated blood pressure (BP) in the setting of an acute aortic emergencies (aneurysm, dissection or other aortic disease).

NCT ID: NCT00805948 Terminated - Clinical trials for Thoracic Aortic Aneurysms

Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thoracic Aortic Aneurysms (THRIVE)

THRIVE
Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the long-term safety and effectiveness of the Talent Thoracic Stent Graft System for treatment of descending thoracic aneurysms (DTA)following U.S. market approval.

NCT ID: NCT00610090 Terminated - Clinical trials for Abdominal Aortic Aneurysms

Safety Study for the Treatment of Abdominal Aortic Aneurysms

UNITE
Start date: May 2007
Phase: Phase 2
Study type: Interventional

The primary study objective, at this time, is to follow out to 5 years post implant the safety of already enrolled subjects who were treated with the UniFit Aorto-uni-iliac (AUI) Endoluminal Stent Graft (the "study device") for the repair of abdominal aortic aneurysms (AAAs).

NCT ID: NCT00546013 Terminated - Hypertension Clinical Trials

Abdominal Aortic Aneurysms and Pseudoexfoliation Syndrome

Start date: December 2001
Phase: N/A
Study type: Observational

Conflicting results have been reported concerning the association of pseudoexfoliation syndrome (PXF) and abdominal aortic aneurysms (AAA). Schumacher et al. reported an association between AAA and PXF, with no consideration of grade. However, a later study did not confirm the association between AAA and PXF. The present study aimed at comparing the relative prevalence of PXF in patients suffering from AAA and in age-matched hypertensive patients.

NCT ID: NCT00508118 Terminated - Clinical trials for Aortic Aneurysm, Thoracic

NICardipine Neuroprotection in AortiC Surgery (NICNACS)

NICNACS
Start date: January 2008
Phase: Phase 2
Study type: Interventional

Objective The objective of this study is to discover whether an infusion of nicardipine is able to reduce the time taken to achieve electrocerebral silence (ECS) during cardiopulmonary bypass (CPB) for aortic surgery. Hypothesis By inhibiting cold-induced cerebral vasoconstriction, nicardipine will maintain cerebral blood flow and allow more rapid cooling of the brain during CPB. This will manifest as a reduction in the time taken to achieve ECS and also as a reduction in overall CPB time.

NCT ID: NCT00444821 Terminated - Clinical trials for ABDOMINAL AORTIC ANEURYSMS

The (PIVOTAL) Study

Start date: March 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to compare endovascular repair using any FDA approved Medtronic AAA Stent Graft System versus surveillance in subjects with smaller abdominal aortic aneurysms (AAA)(4-5CM), with respect to AAA rupture and AAA related deaths.

NCT ID: NCT00409344 Terminated - Sedation Clinical Trials

Dexmedetomidine for Postoperative Sedation in Patients Undergoing Repair of Thoracoabdominal Aortic Aneurysms

Start date: January 2007
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to test the hypothesis that time on the ventilator and ICU length of stay will be shorter in TAA patients given postoperative sedation with dexmedetomidine compared to those given standard sedation. Secondary endpoints are: requirement for sedatives vasoactive drugs incidence of postoperative delirium and cost analysis.

NCT ID: NCT00372138 Terminated - Clinical trials for Abdominal Aortic Aneurysms

Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal Aortic Aneurysms

Start date: September 2006
Phase: N/A
Study type: Interventional

The main risk of aortic aneurysms is rupture that leads to a high risk of death. A preventive surgical treatment is thus needed. In order to reduce the morbidity and mortality associated with conventional surgery, an endovascular approach (insertion of an endovascular stent graft)is now widely favored. The main problem of this procedure is the occurrence of endoleaks (persistence of a communication between the aneurysm and the aorta). A new approach is proposed to prevent these endoleaks. The principle is to draw blood from the patient, separate the blood from the platelets, and reinject both platelet rich plasma (PRP) and autologous thrombin, in order to form a platelet gel (PRP + autologous thrombin). Before studying the efficacy of this technique, its safety of use and feasibility must be evaluated.

NCT ID: NCT00328094 Terminated - Clinical trials for Abdominal Aortic Aneurysm

Glycemic Control to Prevent Cardiac Morbidity in Vascular Surgery

Start date: March 2006
Phase: N/A
Study type: Interventional

Aggressive intraoperative and postoperative management of blood glucose may substantially decrease perioperative cardiovascular and infectious complications in diabetic and non-diabetic patients undergoing vascular surgery. The purpose of this study is to compare the tight versus traditional blood glucose control in diabetics and non-diabetics undergoing vascular surgery in regard to their postoperative fatal and nonfatal cardiac outcomes, and the secondary effects such as rate of infections, overall morbidity and 30-day mortality.