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Aneurysm clinical trials

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NCT ID: NCT01757730 Recruiting - Heart Failure Clinical Trials

Magnetic Resonance Elastography as a Method to Estimate Stiffness of Soft Tissues

MRE
Start date: March 2012
Phase:
Study type: Observational

Magnetic resonance elastography is a novel non-invasive MRI technique to obtain stiffness of soft tissues such as liver, heart, kidneys, etc. In this imaging technique a person is laid in an MR scanner and a paddle (plastic drum) is put on the area of interest to send sound vibration via a speaker placed outside the scan room which is connecting plastic drum via a plastic tube. These vibrations are scanned using MRI to estimate the stiffness of soft tissues such as liver, heart, kidneys, breast etc.

NCT ID: NCT01748903 Recruiting - Clinical trials for Intracranial Aneurysms

TARGET Intracranial Aneurysm Coiling Registry

TARGET
Start date: February 2013
Phase:
Study type: Observational [Patient Registry]

The purpose of this prospective registry is to collect real world, post-marketing data on the use of Stryker Target® 360,Target® 2D, and 2nd generation Target® Nano coils for the embolization of ruptured or unruptured intracranial saccular aneurysms. Up to 300 patients (150 in the TARGET 360°/Helical arm and 150 in the New NANO arm) presenting with intracranial aneurysms suitable for coil embolization will be enrolled at up to 20 sites. A post hoc analysis comparing Target® 360° and Target® 2D coil technical and clinical endpoints will be performed.

NCT ID: NCT01702584 Recruiting - Stent Embolisation Clinical Trials

Efficacy and Safety of StENt-assisted Treatment for CErebral Aneurysms

Start date: September 2012
Phase:
Study type: Observational

Prospective registry study to evaluate safety and efficacy of stent assisted embolization of intracranial aneurysm.

NCT ID: NCT01670903 Recruiting - Hypertension Clinical Trials

The Effect of Angiotensin II Type 1 Receptor Antagonists on the Size and Expansion Rate of Abdominal Aortas in Hypertensive Patients

Start date: May 2011
Phase: N/A
Study type: Observational

Abdominal aortic aneurysm (AAA) is a common disease that develops from degeneration of the aortic wall. The natural history of AAA is gradual expansion and if left untreated may result in rupture and death. The mechanism of the development of this disease is unknown however it appears to be multifactorial and possibly related to degradation processes within the arterial wall. There is growing evidence that Angiotensin receptor blockers ( ARBS) may have an inhibitory effect on remodelling processes within the arterial wall, thus inhibiting degeneration of the vessel wall. Study hypothesis: ARBS are associated with smaller diameters of aortas among hypertensive patients, and are associated with a lower rate of aortic expansion compared to other antihypertensive drugs.

NCT ID: NCT01668563 Recruiting - Clinical trials for Intracranial Hemorrhage Ruptured Aneurysm

International Subarachnoid Aneurysm Trial II

ISAT II
Start date: November 12, 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the clinical outcome of surgical clipping and endovascular coiling for ruptured intracranial aneurysms not included in the original ISAT Study.

NCT ID: NCT01538056 Recruiting - Clinical trials for Abdominal Aortic Aneurysms

Physician Modified Endovascular Grafts

PMEG
Start date: March 2011
Phase: N/A
Study type: Interventional

The primary objectives of this study are to determine whether physician modified endovascular grafts are a safe and effective method of treating patients with elective, symptomatic or ruptured juxtarenal aortic aneurysms in those patients considered to be unsuitable candidates for open surgical repair and have no other options for treatment.

NCT ID: NCT01524211 Recruiting - Clinical trials for Thoracoabdominal Aortic Aneurysm

Evaluation of Branch Endografts in the Treatment of Aortic Aneurysms

Start date: January 25, 2012
Phase: N/A
Study type: Interventional

Zenith t-Branch Study Cohort: The purpose of this study is to collect information on the Cook Zenith t-Branch endovascular stent-graft system and the Terumo Arch Branch for the treatment of aortic aneurysms. Terumo Arch Branch Study Cohort: The purpose of this additional study arm to the current IDE clinical trial is to collect a priori information on the Terumo Arch Branch Endograft for the treatment of proximal thoracic aortic pathologies that cannot be treated with conventional thoracic endografts.

NCT ID: NCT01523262 Recruiting - Aortic Aneurysm Clinical Trials

Preventing Myocardial Ischemia by Preconditioning in Elective Operation for Abdominal Aortic Aneurysm

Start date: January 2011
Phase: Phase 1
Study type: Interventional

Primary To investigate whether peripheral predonditioning induced by brief, intermittent constriction of blood supply to an arm can reduce the incidence of perioperative myocardial ischemia in patients operated electively for infrarenal aortic aneurysm. Secondary To investigate the impact of peripheral preconditioning on perioperative inflammatory response. To investigate whether peripheral preconditoning can protect against perioperative myocardial infarction and reduced cardiac pump function.

NCT ID: NCT01420991 Recruiting - Aneurysm Clinical Trials

Brain and Abdominal Aneurysm Study

BAAS
Start date: August 2011
Phase:
Study type: Observational

Aneurysmal subarachnoid hemorrhage (aSAH) is the most deadly kind of stroke. Each year, 40,000 Americans have SAH. Case-fatality approaches 60% and more than half of those who die do so before reaching the hospital. Most commonly, SAH results from rupture of an intracranial aneurysm. Screening high-risk individuals could identify those at greatest risk and decrease the devastating effect of SAH. Aortic Aneurysm also constitutes a major public health problem with high lethality. Current estimates are that ruptured aortic aneurysm kills 13,000 Americans each year. Screening efforts have effectively lowered mortality from aortic aneurysm rupture but a high proportion of those who die did not have a diagnosis of aortic aneurysm prior to rupture. The relationship between intracranial and aortic aneurysm has long been recognized, but poorly quantified. Recent genome-wide association studies (GWAS) provide a molecular biological evidence for a shared pathophysiology. The chromosome 9p21 locus confers increased risk for both intracranial aneurysms and aortic aneurysms. These GWAS data, along with linkage data for other susceptibility loci, indicate that individuals and families harboring one type of aneurysm may be at especially increased risk of the other. The rationale for this project is that opportunistic screening for abdominal aortic aneurysms (AAA) may be warranted in patients who present with aneurysmal subarachnoid hemorrhage. This study is meant to see if the yield of screening in this population is too low to justify its routine use. The investigators plan to systematically screen for AAA in all cases of aSAH presenting to MCH for treatment. If no individual out of 81 consecutively screened cases of aSAH has evidence of AAA, then the investigators can have strong confidence that there is a less than 5% chance of finding an AAA in the patient population.

NCT ID: NCT01291290 Recruiting - Clinical trials for Ruptured Abdominal Aortic Aneurism

START - Early Thrombocyte Administration to Patients With Ruptured Abdominal Aortic Aneurism

rAAA
Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of platelet infusion prior to transfer to a vascular surgical department in patients with a ruptured abdominal aortic aneurism.