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Aneurysm clinical trials

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NCT ID: NCT00821145 Withdrawn - Clinical trials for Infra and Juxtarenal Abdominal Aortic Aneurysms

Laparoscopic Versus Open Abdominal Aortic Aneurysm (AAA) Exclusion

LapAorta
Start date: January 2009
Phase: Phase 3
Study type: Interventional

In many countries the gold standard for treating abdominal aortic aneurysms is still open surgery with a long incision. In patients with suitable anatomy alternatively an endovascular approach can be chosen. Since open surgery is more durable in many countries a laparoscopic procedure using " key hole surgery " has gained wider acceptance. The current study wants to prove that laparoscopic aortic aneurysm procedures are less invasive than open surgery with reduced recovery times.

NCT ID: NCT00816062 Completed - Clinical trials for Aortic Aneurysm, Abdominal

Post-Approval Trial of the Talentâ„¢ Abdominal Stent Graft to Treat Aortic Aneurysms

VITALITY
Start date: December 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to examine, through the endpoints established in this protocol, the long-term safety and effectiveness of the Talent Abdominal Stent Graft System, in a post-approval environment.

NCT ID: NCT00813358 Completed - Clinical trials for Descending Thoracic Aortic Aneurysm

Zenith TX2® Post-market Approval Study

TX2 2PAS
Start date: July 10, 2009
Phase: N/A
Study type: Interventional

The Zenith TX2® Post-market Approval Study is a clinical trial approved by US FDA to further study the safety and effectiveness of the Zenith TX2® TAA Endovascular Graft in the treatment of thoracic aortic aneurysms.

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: NCT00803075 Completed - Clinical trials for Aortic Aneurysm, Abdominal

Endovascular Repair of Abdominal Aortic Aneurysms

Start date: February 2002
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if it is safe and effective to use the TALENT AAA Stent Graft System as a treatment for AAAs in patients who are also candidates for conventional surgical aneurysm repair.

NCT ID: NCT00802984 Completed - Clinical trials for Aortic Aneurysm, Thoracic

Endovascular Repair of Descending Thoracic Aortic Aneurysms

Start date: January 2002
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the system is safe and effective for the intended use of treating descending thoracic aortic aneurysms.

NCT ID: NCT00794092 Completed - Aortic Aneurysm Clinical Trials

Magnetic Resonance Imaging of Aortic Aneurysm Instability

Start date: November 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Abdominal aortic aneurysm (AAA) is a progressive enlargement of the aorta, the largest blood vessel in the body. It is at risk of bursting when it is usually fatal. Currently the risk of the AAA bursting is estimated from its diameter. In this study, the investigators hope to develop a new type of aneurysm scan involving Magnetic Resonance Imaging (MRI). It is hoped that this scan will be better at determining which AAAs are at risk of bursting and therefore require an operation to prevent this.

NCT ID: NCT00777907 Completed - Clinical trials for Intracranial Aneurysm

Complete Occlusion of Coilable Aneurysms

COCOA
Start date: October 2008
Phase: Phase 3
Study type: Interventional

To compare the safety and effectiveness of Pipeline Embolization Device to coil embolization for the treatment of coilable wide-necked intracranial aneurysms

NCT ID: NCT00777088 Completed - Clinical trials for Intracranial Aneurysm

Pipeline for Uncoilable or Failed Aneurysms

PUFS
Start date: October 2008
Phase: N/A
Study type: Interventional

To determine the safety and effectiveness of Pipeline Embolization Device for the treatment of uncoilable or failed wide-necked intracranial aneurysms (IA).

NCT ID: NCT00757133 Completed - Aortic Aneurysm Clinical Trials

Prevention of Incisional Hernia by Mesh Augmentation After Midline Laparotomy for Aortic Aneurysm Treatment

PRIMAAT
Start date: November 2008
Phase: N/A
Study type: Interventional

The research hypothesis for this study is to possibly reduce the incidence of incisional hernia 2 years postoperatively after midline laparotomy for treatment of aortic aneurysm from 25% to 5% by mesh augmentation during closure of the laparotomy. The study is designed as a prospective randomised multi-centre trial, randomising patients in 2 groups concerning the surgical technique of the closure of the abdominal wall.