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Aortic Aneurysm, Abdominal clinical trials

View clinical trials related to Aortic Aneurysm, Abdominal.

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NCT ID: NCT00583050 Completed - Clinical trials for Abdominal Aortic Aneurysm

Endovascular Exclusion of TAAA/AAA Utilizing Fenestrated/Branched Stent Grafts

Start date: February 2001
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the role of fenestrated/branched stent-grafts in the exclusion of abdominal aortic and thoracoabdominal aneurysms.

NCT ID: NCT00549432 Active, not recruiting - Clinical trials for Abdominal Aortic Aneurysm

Clinical Study of Abdominal Aortic Aneurysm Exclusion (TALENT Abdominal)

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Start date: October 2002
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the TALENT endoluminal stent-graft system in patients with abdominal aortic aneurysms. The TALENT endoluminal stent-graft system is a flexible, implantable endoluminal vascular device preloaded in a placement system that is used to exclude abdominal aortic aneurysms.

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: NCT00543270 Completed - Clinical trials for Abdominal Aortic Aneurysm

Powerlink Bifurcated Stent Graft Long-Term Follow-up Study

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

Endologix Infrarenal Bifurcated Stent Graft Study

NCT ID: NCT00538967 Completed - Clinical trials for Aortic Aneurysm, Abdominal

The Effect of Doxycycline on Matrix Metalloproteinase Expression and Activity in the Abdominal Aneurysm

Start date: May 2002
Phase: Phase 2
Study type: Interventional

The matrix metalloproteinase-9 (MMP-9) is considered to play a central role in abdominal aortic aneurysm (AAA) initiation. Doxycycline has direct MMP-9 inhibiting properties in vitro, and it effectively suppresses AAA development in rodents. Observed inhibition of AAA progression, and contradictory findings in human studies evaluating the effect of doxycycline therapy on aortic wall MMP-9 suggest that the effects of doxycycline extend beyond MMP-9 inhibition, and that the effect may be dose dependent.

NCT ID: NCT00538421 Completed - Surgery Clinical Trials

Opioid-potentiated Volative Anaesthetic Vs. Remifentanil And Propofol During Abdominal Aortic Aneurysm Surgery

ABSENT
Start date: March 2008
Phase: Phase 4
Study type: Interventional

Comparing 2 different anaesthetic methods during abdominal aortic aneurysm surgery. The patients will be followed up 30 days postoperative. Number of patients included will be 200. Perioperative details will be analyzed.

NCT ID: NCT00522535 Completed - Clinical trials for Abdominal Aortic Aneurysms

Prospective Aneurysm Trial: High Angle Aorfix™ Bifurcated Stent Graft

PYTHAGORAS
Start date: April 2006
Phase: N/A
Study type: Interventional

Purpose of this study: The purpose of the study is to evaluate the safety and effectiveness of the Lombard Medical endovascular Aorfix™ AAA bifurcated stent graft in the treatment of abdominal aortic, aorto-iliac and common iliac aneurysms with anatomies including angled aorta, angled aneurysmal body, or both, between 0° and 90°. Study hypothesis: The primary efficacy hypothesis is the proportion of grafts remaining free from endoleak, migration, and fracture at 12 months. Efficacy: The 12 month, all cause mortality rate in the Aorfix™ group will be non-inferior to the 12 month, all cause mortality rate in the Open Control group. Safety: The rates of early serious adverse events between 0 and 30 days post-operative in the Aorfix™ groups will be non-inferior to the early serious adverse event rates between 0 and 30 days post-operative in the Open Control group.

NCT ID: NCT00513773 Completed - Clinical trials for Aortic Aneurysm, Abdominal

Inflammation and Risk Prediction in Patients With Abdominal Aortic Aneurysm

Start date: July 2008
Phase: N/A
Study type: Observational

The purpose of this study is to better understand the role of inflammation in the pathophysiology of abdominal aortic aneurysm. In this study we hope to show better ways of predicting risk in this condition by using a combination of FDG-PET with CT.

NCT ID: NCT00507559 Completed - Clinical trials for Abdominal Aortic Aneurysms (AAA)

The Pivotal Study of the Aptus Endovascular AAA Repair System

STAPLE-2
Start date: September 2007
Phase: N/A
Study type: Interventional

A prospective, non-randomized, multi-center clinical study to evaluate the safety and effectiveness of the Aptus Endovascular AAA Repair System compared to an open surgical repair historical control group in the treatment of abdominal aortic aneurysms (AAA).

NCT ID: NCT00493389 Recruiting - Clinical trials for Aortic Aneurysm, Abdominal

Cortisol Response to Adrenocorticotrophin (ACTH) in Acute Stress

CRAAS
Start date: July 2007
Phase: N/A
Study type: Interventional

Cortisol deficiency is diagnosed by the adrenocorticotrophin (ACTH) stimulation test. This test measures cortisol levels in the blood before and after giving an injection of ACTH. Currently, the results of this test can only be reliably interpreted when it is carried out on people in non-stressful situations. Frequently the test is carried out in hospitalized patients in stressful situations, giving results that are hard to interpret. Our study is to first do this test in a non-stressful situation, followed by a repeat test in a stressful situation, to compare the results and create a set of guidelines for interpreting the test when it is carried out in stressful situations.