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Aneurysm clinical trials

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NCT ID: NCT00421330 Active, not recruiting - Clinical trials for Abdominal Aortic Aneurysm

Dutch Randomised Endovascular Aneurysm Management (DREAM-) Trial

Start date: November 2000
Phase: N/A
Study type: Interventional

The purpose of this trial is to assess whether the new endovascular repair technique of the abdominal aortic aneurysm (AAA) is an adequate substitute of the conventional AAA repair.

NCT ID: NCT00416000 Completed - Clinical trials for Abdominal Aortic Aneurysm

Mechanism and Prevention of Remote Organ Injury Following Ruptured Aortic Aneurysm

Start date: January 2006
Phase: N/A
Study type: Observational

It has been estimated that 80% of deaths from abdominal aortic aneurysms results from rupture. Endovascular Aneurysm Repair (EVAR) has been applied to RAAA (Ruptured Abdominal Aortic Aneurysm) patients with reports of improvements. Despite the use of EVAR, patients have developed complications with lung and kidney function. This study will investigate certain biochemical processes that will potentially reduce these complications. Knowledge gained from this study may also be used to further research in this field through larger studies.

NCT ID: NCT00413231 Completed - Clinical trials for Thoracic Aortic Aneurysm

Valor II: The Valiant Thoracic Stent Graft System Clinical Study

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

This study was designed to study safety and effectiveness of the Valiant Thoracic Stent Graft to treat thoracic aortic aneurysms.

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: NCT00396981 Completed - Clinical trials for Intracranial Aneurysms

MAPS Trial: Matrix And Platinum Science

MAPS
Start date: March 2007
Phase: Phase 4
Study type: Interventional

Primary Objectives: - To establish Target Aneurysm Recurrence (TAR) rates for Matrix 2® and GDC® Coils used for the treatment of intracranial saccular aneurysms. TAR is defined as clinically relevant recurrence resulting in: target aneurysm reintervention, rupture/re-rupture and/or death from an unknown cause. - To correlate defined angiographic endpoints with TAR rates and assess their predictive value, thereby providing a framework to establish clinically relevant endpoints for future studies. Secondary Objectives: - To evaluate device characteristics, incidence and severity of device-related adverse events, including death, neurological deterioration and changes in functional abilities. - To establish angiographic recurrence rates for Matrix 2® and GDC® Coils used for the treatment of intracranial saccular aneurysms. - To explore an experimental, quantitative and volumetric endpoint and correlate these with existing qualitative assessments.

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: NCT00358085 Not yet recruiting - Clinical trials for Aortic Aneurysm, Abdominal

NExT ERA: National Expertise Based Trial of Elective Repair of Abdominal Aortic Aneurysms: A Pilot Study

Start date: September 2006
Phase: Phase 3
Study type: Interventional

Objectives. To study the feasibility of an expertise-based randomized controlled trial (RCT) testing the role of traditional surgery (OPEN) versus endovascular repair (EVAR) for abdominal aortic aneurysms (AAA). Study design. We will conduct an expertise-based RCT comparing OPEN to EVAR of non-urgent abdominal aortic aneurysms in patients referred to vascular surgeons practicing at Hamilton Health Sciences, to determine the rate of death and other complications. Quality of life and status at 6 months will also be recorded. The ultimate goal is to determine the feasibility of conducting a pragmatic expertise-based RCT and to inform a future larger study at a national level.

NCT ID: NCT00349947 Completed - Clinical trials for Aortic Aneurysm, Abdominal

Exercise Therapy to Treat Adults With Abdominal Aortic Aneurysms

AAA:STOP
Start date: November 2006
Phase: Phase 1
Study type: Interventional

An abdominal aortic aneurysm (AAA) is a weakened and enlarged area in the abdominal aorta, which is a large blood vessel in the abdomen. If an AAA ruptures, it can be life-threatening. Research has shown that sedentary individuals are at increased risk of developing AAAs. This study will evaluate the effectiveness of an exercise program at limiting the growth of small AAAs in older individuals.

NCT ID: NCT00349908 Completed - Atherosclerosis Clinical Trials

A Feasibility Study of the Cordis Neurovascular Self Expanding Stent System in Intracranial Arteries

Start date: September 2006
Phase: Phase 1
Study type: Interventional

Feasibility study to assess safety of treating patients with self expanding stent in intracranial arteries.

NCT ID: NCT00339053 Recruiting - Clinical trials for Respiratory Insufficiency

Immunonutrition and Thoracoabdominal Aorta Aneurysm Repair

Start date: September 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether immunonutrition and pre operative nutrition can reduce lenght of respirator support, lenght of stay in the ICU and incidence of post operative infections