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Aneurysm clinical trials

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NCT ID: NCT01756833 Completed - Aneurysm Clinical Trials

Non-Invasive Treatment of Abdominal Aortic Aneurysm Clinical Trial

N-TA^3CT
Start date: May 2013
Phase: Phase 2
Study type: Interventional

The primary aim of this study is to determine if doxycycline (100 mg bid) will inhibit (by at least 40%) the increase in greatest transverse diameter of small abdominal aortic aneurysms (3.5-5.0 cm in men, 3.5-4.5 cm in women) over a 24-month period of observation in comparison to a placebo-treated control group.

NCT ID: NCT01754051 Completed - Clinical trials for Intracranial Aneurysms

A Volumetric Coiling in Aneurysm Registry of the Penumbra Coil 400TM System

VOLCAN
Start date: January 2013
Phase:
Study type: Observational [Patient Registry]

This study is a prospective, multi-center registry of patients with intracranial aneurysms who are treated by the PC 400 System. Data for each patient are collected up to 12 ± 3 months post-procedure for the study.

NCT ID: NCT01740700 Completed - Clinical trials for Aortic Aneurysm, Abdominal

Zenith® p-Branch® OTS Multicenter Study

Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of the Zenith® p-Branch® OTS Multicenter Study is to provide an early clinical experience and evaluate the safety and effectiveness of the Zenith® p-Branch® in the treatment of pararenal or juxtarenal abdominal aortic aneurysms (AAA).

NCT ID: NCT01726257 Completed - Clinical trials for Abdominal Aortic Aneurysm (AAA)

Safety and Effectiveness Study of Endovascular Abdominal Aortic Aneurysm Repair Using the Nellix® System

EVAS IDE
Start date: December 2013
Phase: N/A
Study type: Interventional

The objective of this study is to assess the safety and effectiveness of the Endologix Nellix® System for the endovascular repair of infrarenal abdominal aortic aneurysms (AAA).

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: NCT01716117 Completed - Brain Aneurysm Clinical Trials

Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Treating Large or Giant Wide Neck Aneurysms

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

This clinical research study is designed to determine safety and effectiveness of the Surpass Flow Diverter (Surpass System), an investigational device developed to treat wide-neck, large or giant intracranial aneurysms. An intracranial aneurysm is a bulge in the wall of a blood vessel in the brain. The bulge is caused by a weakening of the vessel wall. If left untreated, the bulge may continue to grow larger and ultimately the vessel may break open (rupture), resulting in serious bleeding into or around the brain. The information collected from this study will be used to evaluate how well patients do when treated with the Surpass System both immediately after treatment of an aneurysm and over a long period of time (5 years).

NCT ID: NCT01710072 Completed - Clinical trials for The Focus of the Study is to Monitor MRI Signal Changes and Inflammatory Biomarkers With Use of Aspirin in Patients With Unruptured Cerebral Aneurysm

Aspirin Attenuates Inflammation in Human Cerebral Aneurysms

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

Hypothesis: aspirin attenuates inflammation in cerebral aneurysms and hence reduces the incidence of rupture. This effect can be monitored using the signal generated by macrophages (inflammatory biomarker) in ferumoxytol-enhanced MRI. Study aims: 1. Determine if daily aspirin intake (for three months) would obliterate/reduce ferumoxytol-enhanced MRI signal changes generated by macrophages in cerebral aneurysm wall. Fifteen patients with cerebral aneurysms > 7 mm will be selected to enroll in this pilot study. 10 patients will be imaged at base line with ferumoxytol-enhanced MRI. Following that, they will take aspirin 81 mg daily and then re-imaged again at three months. This group will be compared to a control group of 5 patients where they will have the imagings studies performed at base line and at three months but will NOT take aspirin.

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: 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.