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Constriction, Pathologic clinical trials

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NCT ID: NCT01941420 Completed - Aortic Stenosis Clinical Trials

Comparison of Blood and Crystalloid Cardioplegia

Start date: November 2006
Phase: N/A
Study type: Observational [Patient Registry]

The investigators decided to make a study with a cohort of patients as homogenous as possible with a cross clamp time around 70 min. Adult patients with a severe aortic stenoses without any other significant heart disease was included in our prospective randomised study. This group of patients was chosen for two reasons. First, these patients have left ventricular hypertrophy making the myocardium vulnerable to ischemia, secondly the investigators wanted to avoid the possible confounding effect of ischemia found in patients with variable degrees of coronary artery disease. Therefore, patients with additional significant coronary artery disease (≥ 50% stenoses) were excluded from the study.

NCT ID: NCT01923740 Completed - Clinical trials for Coronary Artery Disease

A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) System in Chinese Population ~ ABSORB CHINA Randomized Controlled Trial (RCT)

ABSORB CHINA
Start date: July 2013
Phase: N/A
Study type: Interventional

To evaluate the safety and efficacy of the Absorb BVS System compared to the XIENCE V Everolimus Eluting Coronary Stent System (EECSS) in the treatment of subjects with ischemic heart disease caused by up to two de novo native coronary artery lesions in separate epicardial vessels.

NCT ID: NCT01901874 Completed - Clinical trials for Carotid Artery Stenosis

The Gore SCAFFOLD Clinical Study

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

Evaluate the safety and efficacy of the GORE® Carotid Stent for the treatment of carotid artery stenosis in patients at increased risk for adverse events from carotid endarterectomy

NCT ID: NCT01899300 Completed - Clinical trials for Refractory Benign Esophageal Strictures Caused by Caustic Ingestion

Esophageal Fully Covered Metal Stents in Caustic Strictures Study

Start date: March 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to establish clinical proof of concept of temporary indwell of the WallFlex™ Esophageal Fully Covered Metal Stent (FCMS) for the treatment of refractory benign esophageal strictures caused by caustic ingestion.

NCT ID: NCT01888536 Completed - Clinical trials for Neurologic Claudication in Patients With Lumbar Spinal Stenosis

A Study to Evaluate Efficacy of 『Opast Tablet』for Neurologic Claudication in Patients With Lumbar Spinal Stenosis

Start date: February 2013
Phase: Phase 4
Study type: Interventional

This trial is a comparative study of Opast tablet and Rikalin capsule 75mg and Rikalin capsule 75mg in combination with Opast tablet to evaluate improvement effectiveness of Opast tablet on subjective symptoms and neurologic claudication in patients with lumbar spinal stenosis.

NCT ID: NCT01845207 Completed - Aortic Stenosis Clinical Trials

Frailty Assessment Before Cardiac Surgery & Transcatheter Interventions

Start date: January 2012
Phase: N/A
Study type: Observational [Patient Registry]

Frailty is a state of decreased physiologic reserves and vulnerability to stressors. Several tools exist to measure frailty, some based on physical tests and others on questionnaires, yet there is no agreement on which tool to recommend. This multi-center prospective cohort study is aimed at comparing various frailty assessment tools to determine which best predicts death or major complications after cardiac surgery or transcatheter intervention. The population of interest is elderly patients with severe aortic stenosis undergoing surgical or transcatheter aortic valve replacement. The frailty assessment tools under investigation include composite frailty scales, physical performance tests, muscle mass, and biomarker expression. The overall objective is to improve our ability to predict risk by measuring frailty using the optimal tool in elderly cardiovascular patients.

NCT ID: NCT01843582 Completed - Clinical trials for Generalized Visual Field Contraction or Constriction

A Study to Determine the Location of the Blind Spot and the Macula-disc Centre Distance on a Fundus Photograph

Start date: May 2013
Phase: N/A
Study type: Observational [Patient Registry]

The study is aimed to develop a new reaction-time based method for examining the visual field and to study the effect of refractive error on the magnification of a fundus photograph in order to evaluate the true size of a retinal feature.

NCT ID: NCT01843426 Completed - Clinical trials for Aortic Valve Stenosis

Aortic Stenosis Pre-Transcatheter Aortic Valve Replacement (TAVR) Procedure CT Scan

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

The purpose of this study is to evaluate contrast media volume, safety and 30-day outcome of patients after a computed tomography (CT) scan. The results of this study will help to determine the minimum volume of contrast material that can be used to ensure patient safety while not compromising diagnostic image quality in high-risk patients.

NCT ID: NCT01840540 Completed - Clinical trials for Renovascular Hypertension

MSC for Occlusive Disease of the Kidney

Start date: April 2013
Phase: Phase 1
Study type: Interventional

To determine the safety and toxicity of intra-arterial infused autologous adipose derived mesenchymal stromal (stem) cells in patients with vascular occlusive disease of the kidney.

NCT ID: NCT01837160 Completed - Aortic Stenosis Clinical Trials

Angiogenesis and Fibrosis in Aortic Stenosis

Start date: April 2013
Phase: N/A
Study type: Observational

Angiogenesis and fibrosis lie at the heart of a number of fundamental processes responsible for cardiovascular disease. In this proposal, the investigators intend to build upon a highly successful programme of studies exploring the cardiovascular applications of positron emission tomography. Specifically, the investigators will explore the potential role of a novel radiotracer, 18F-fluciclatide, which is a highly selective ligand for the αvβ3 and αvβ5 integrin receptors that are up regulated during angiogenesis, and tissue fibrosis and remodelling. This tracer has been successfully used to assess angiogenesis in metastatic tumours and its uptake is suppressed by anti-angiogenic therapies. The investigators here propose to describe the pattern of uptake of 18F-fluciclatide in cardiovascular diseases, specifically aortic stenosis and aortic atherosclerosis. The investigators will correlate 18F-fluciclatide uptake with in vivo measures of angiogenesis and fibrosis as well as ex vivo histological characterisation of tissue. If successful, this novel radiotracer could provide an extremely important non-invasive method of assessing in vivo angiogenesis, plaque vulnerability, and tissue remodelling as well as potential applications in developing stem cell therapies.