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Aneurysm clinical trials

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NCT ID: NCT00488943 Recruiting - Clinical trials for Abdominal Aortic Aneurysm

Follow-up After Endovascular Repair of Abdominal Aortic Aneurysm

Start date: January 2005
Phase:
Study type: Observational

To collect and analyze clinical follow-up data which can be used to assess the safety, efficacy, and durability of endovascular AAA repair with Zenith and Chuter-Gianturco stent-grafts.

NCT ID: NCT00488696 Recruiting - Clinical trials for Aortic Aneurysm of the Proximal Arch

Branched Aortic Arch Study

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

This is a study to assess the safety and effectiveness of endovascular treatment of aortic aneurysms involving the proximal aortic arch. The investigational operation involves placing a stent-graft over the aortic aneurysm.

NCT ID: NCT00488358 Completed - Clinical trials for Abdominal Aortic Aneurysm

Hemodynamic Changes After Aortic Aneurysm Treatment With Stent-Graft

Start date: November 2005
Phase: N/A
Study type: Observational

To compare the aortic pulse profile before and after stent-graft implantation to prove that endovascular AAA repair using non-compliant stent-graft changes the aortic pulse profile.

NCT ID: NCT00486226 Completed - Clinical trials for Intracranial Aneurysm

The Registry to Study Safety and Performance of the CORDIS Vascular Reconstruction Device and Delivery System

SUNRISE
Start date: June 1, 2007
Phase:
Study type: Observational

The objective of the registry is to evaluate the real world safety and performance of the CORDIS ENTERPRISE™ Vascular Reconstruction Device and Delivery System (VRD) to facilitate endovascular coil embolization of intracranial aneurysms.

NCT ID: NCT00483249 Recruiting - Clinical trials for Thoracoabdominal Aortic Aneurysm

Endovascular Exclusion of Thoracoabdominal and/or Paravisceral Abdominal Aortic Aneurysm

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

This is a study to assess the safety and effectiveness of endovascular treatment of thoracoabdominal (TAAA) and paravisceral abdominal (PVAAA) aortic aneurysms. The investigational operation involves placing a stent-graft over the aortic aneurysm.

NCT ID: NCT00478803 Completed - Aortic Aneurysm Clinical Trials

Conservative Aortic Valve Surgery for Aortic Insufficiency and Aneurysms of the Aortic Root. CAVIAAR

CAVIAAR
Start date: May 2007
Phase: Phase 3
Study type: Interventional

The primary objective of the CAVIAAR study is to prove that aortic valve sparing for patients with aortic root aneurysms and/or dystrophic aortic insufficiency is associated with a 45% increase of 3 years-survival rate without increased mortality or serious increased morbidity events when compared to mechanical valve replacement. The main hypothesis of this study is that a standardized procedure of valve sparing based on external aortic annuloplasty in patients with dystrophic aortic insufficiency and/or aortic root aneurysm increases survival rate without increased mortality or serious increased morbidity events when compared with patients undergoing mechanical aortic valve replacement.

NCT ID: NCT00449306 Active, not recruiting - Atherosclerosis Clinical Trials

Physical,Histological,and Genetic Analyses of Lipid-rich Atherosclerotic Plaques

Start date: March 2001
Phase:
Study type: Observational

Lipid-rich atherosclerotic plaques, or "vulnerable plaques" are prone to rupture, causing local intravascular thrombosis, with subsequent grave clinical consequences. Atherosclerotic plaques normally removed during surgery, and peripheral blood samples will be studied to achieve the following objectives: "1" Define histological features of the vulnerable plaque, analyze its physical characteristics, and investigate selected gene expression. "2" Study biomarkers of inflammation in conjunction with the presence of vulnerable plaques. "3" Explore the potential role of infection in atherogenesis.

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: NCT00442065 Completed - Clinical trials for Abdominal Aortic Aneurysm

ARBITER-II: Aorfix™ Bifurcated Safety and Performance Trial: Phase II, Angulated Vessels

ARBITER-II
Start date: October 2006
Phase: Phase 2/Phase 3
Study type: Interventional

To assess the safety and performance of Aorfix™ Stent Grafts in the treatment of Abdominal Aortic and Aorto-Iliac Aneurysm where a significant degree of vessel angulation exists at the neck of the aneurysm or in the common iliac arteries.

NCT ID: NCT00435942 Completed - Clinical trials for Thoracic Aortic Aneurysms

Phase II Study of the Safety and Efficacy of the Relay Thoracic Stent-Graft

Start date: January 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of the Relay thoracic stent-graft system to treat thoracic aortic aneurysms. Efficacy will be evaluated by the device-related adverse event rate of endovascular repair (via Relay Thoracic Stent-Graft) through 1-year. Safety will be evaluated by comparing major adverse events through 1-year in subjects treated with the Relay Thoracic Stent-Graft to those who underwent surgical repair. Long term follow-up is conducted through 5 years.