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Aortic Aneurysm clinical trials

View clinical trials related to Aortic Aneurysm.

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NCT ID: NCT01723618 Completed - Clinical trials for Abdominal Aortic Aneurisms

Pharmacokinetics of CRD007 in Patients With Abdominal Aorta Aneurisms.

Start date: November 2012
Phase: Phase 1
Study type: Interventional

The purpose of the study is to determine the plasma levels of CRD007 in patients with abdominal aortic aneurysms after the administration of single doses of tablets containing 10, 25 and 40 mg CRD007.

NCT ID: NCT01710878 Completed - Clinical trials for Abdominal Aorta Aneurysm

Performance and Safety of a Second Generation Antimicrobial Graft in Abdominal Position

SYNERGY
Start date: February 2008
Phase: N/A
Study type: Interventional

Safety and performance of an anti-microbial vascular graft in the treatment of aneurysmal and occlusive disease of the abdominal aorta.

NCT ID: NCT01704391 Completed - Acute Kidney Injury Clinical Trials

Haemodynamic Response to Aortic Surgery

Start date: January 2012
Phase:
Study type: Observational

Open elective abdominal aortic surgery is a high risk procedure involving clamping of the aorta. Indications include abdominal aortic aneurysm (AAA) or aortic occlusive disease (AOD) causing lower limb ischaemia. These patients are often regarded as one entity in postoperative study settings. However, previous studies indicate that risk profiles, inflammatory activity, and haemodynamic capacity may differ between these groups. The first aim of this study was to evaluate postoperative ICU-requirements after open elective abdominal aortic surgery, hypothesising that AAA-patients had longer ICU-stays and needed more mechanical ventilation or acute dialysis than did patients with AOD. The investigators see a relatively high incidence of postoperative acute kidney injury (AKI) following aortic surgery. Neutrophil Gelatinase Associated Lipocalcin (NGAL) may be useful in the early diagnosis of postopeative AKI. However, NGAL is also known as a marker of inflammatory activation. The ischaemia-reperfusion injury and subsequent inflammatory response to aortic cross clamping may per se induce a rise in NGAL despite intact renal function. Therefore NGAL may not be a reliable marker of AKI after AAS. The second aim of this study is to describe the changes in NGAL after AAS in patients with and without postoperative dialysis-dependent AKI.

NCT ID: NCT01704300 Completed - Stroke Clinical Trials

Body Mass Index and Initial Presentations of Cardiovascular Diseases

CALIBER
Start date: January 2001
Phase: N/A
Study type: Observational

The association between obesity and cardiovascular disease (CVD) has mostly been studied using broad endpoints or have focused on cause-specific mortality. The investigators aim to compare the effect of body mass index (BMI) on different types of initial presentation of CVD.

NCT ID: NCT01698671 Active, not recruiting - Clinical trials for Aortic Aneurysm, Abdominal

InterGard Synergy Post-Marketing Surveillance Study

Start date: October 2012
Phase: N/A
Study type: Interventional

The purpose of the study is to assess the performance and safety of the InterGard Synergy vascular graft.

NCT ID: NCT01691911 Completed - Clinical trials for Abdominal Aortic Aneurysm

Preconditioning Shields Against Vascular Events in Surgery

SAVES
Start date: February 2012
Phase: N/A
Study type: Interventional

Major vascular surgery involves operations to repair swollen blood vessels, clear debris from blocked arteries or bypass blocked blood vessels. Patients with these problems are a high-risk surgical group as they have generalized blood vessel disease. These puts them at risk of major complications around the time of surgery such as heart attacks , strokes and death. The mortality following repair of a swollen main artery in the abdomen is about 1 in 20. This contrasts poorly with the 1 per 100 risk of death following a heart bypass. Simple and cost-effective methods are needed to reduce the risks of major vascular surgery. Remote ischaemic preconditioning (RIPC) may be such a technique. To induce RIPC, the blood supply to muscle in the patient's arm is interrupted for about 5 minutes. It is then restored for a further five minutes. This cycle is repeated three more times. The blood supply is interrupted simply by inflating a blood pressure cuff to maximum pressure. This repeated brief interruption of the muscular blood supply sends signals to critical organs such as the brain and heart, which are rendered temporarily resistant to damage from reduced blood supply. Several small randomized clinical trials in patients undergoing different types of major vascular surgery have demonstrated a potential benefit. This large, multi-centre trial aims to determine whether RIPC can reduce complications in routine practice.

NCT ID: NCT01683084 Completed - Clinical trials for Abdominal Aortic Aneurysm

Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdominal Aortic Aneurysms

TEDY
Start date: September 19, 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if telmisartan is effective in slowing the progression of abdominal aortic aneurysms and reducing circulating concentrations of Abdominal Aortic Aneurysms (AAA) biomarkers.

NCT ID: NCT01681251 Completed - Clinical trials for Abdominal Aortic Aneurysm Uncomplicated

Goal Directed Therapy for Patients Undergoing Major Vascular Surgery

Start date: August 2010
Phase: Phase 1
Study type: Interventional

The management and delivery of intravenous fluids during surgical operations is one of the important duties for anesthesiologists. The goal of this study was to determine if goal directed fluid therapy, titrated using the FloTrac monitor's measurement of stroke volume variation results in a decrease in the length of stay of patients undergoing open abdominal aneurysm repair.

NCT ID: NCT01679288 Completed - Hypertension Clinical Trials

Screening for Abdominal Aortic Aneurysm and Abdominal Aortic Atherosclerosis by Hand-Held Ultrasonography

ECO-AAA
Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the prevalence of abdominal aortic aneurysm (AAA) and abdominal aortic atheromatosis (AA-At) using a hand-held ultrasound by a general practitioner in Primary Health Care.

NCT ID: NCT01678274 Active, not recruiting - Hypertension Clinical Trials

Prospective Characterization of the Heart, Aorta and Blood Pressure in Turner Syndrome. Association With Aortic Dissection.

TSCORII
Start date: December 2013
Phase: N/A
Study type: Observational

Turner syndrome is a congenital complete or partial lack one of the female sex chromosomes affecting 1 of 2000 live born girls. The syndrome is characterized by an increased prevalence of ischemic heart disease, aortic dilation and dissection, hypertension, stroke and autoimmune diseases in general. Our study aim is: - Using MRI to further characterize and find risk factors leading to aortic dilation. - Using MRI to assess the degree of aortic distensibility. - Using Computed tomography x-ray scanning of the heart and coronary arteries to characterize the prevalence and degree of ischemic heart disease and coronary anomalies. - Using pressure sensitive ultrasound (applanation tonometry) to assess the degree of aortic stiffness when compared to controls using end points as Pulse Wave Velocity, Augmentation Index and Central Pulse Pressure.