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Constriction, Pathologic clinical trials

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NCT ID: NCT00535899 Terminated - Aortic Stenosis Clinical Trials

Speckle Tracking Imaging in Patients With Low Ejection Fraction Aortic Stenosis (SPArKLE-AS)

SPArKLE-AS
Start date: September 2007
Phase: N/A
Study type: Observational

In patients with aortic stenosis and low ejection fraction, how can we predict who will recover their ejection fraction after aortic valve replacement? We plan to observe 50 patients with Low EF aortic stenosis and perform serial echocardiograms pre and post-aortic valve replacement and analyze regional wall motion contractility with a new software application called speckle tracking imaging.

NCT ID: NCT00529997 Terminated - Clinical trials for Lumbar Spinal Stenosis

Dynamic Stabilization for Lumbar Spinal Stenosis With Stabilimax NZ® Dynamic Spine Stabilization System

Start date: February 2007
Phase: N/A
Study type: Interventional

The purpose of this trial is to assess whether the Stabilimax NZ® is at least as safe and effective as the control therapy of fusion in patients receiving decompression surgery for the treatment of clinically symptomatic spinal stenosis at one contiguous vertebral levels from L1-S1. Safety and effectiveness will be assessed by means of primary study endpoints which address improvements in pain and function in the absence of major device related complications. The study hypothesis criteria for demonstrating safety and efficacy requires scientific evidence that patients classified as satisfying the primary study endpoint post device implantation is at least as good for Stabilimax NZ® recipients as that for patients undergoing fusion with posterior pedicle screw instrumentation at the 24 month followup assessment.

NCT ID: NCT00517751 Terminated - Clinical trials for Lumbar Spinal Stenosis

Condition of Approval Study

COAST
Start date: August 2007
Phase: Phase 4
Study type: Interventional

This prospective, multicenter longitudinal five-year study of X-STOP PEEK usage in LSS patients is designed to supplement pre-market safety and effectiveness data with information on longer-term device performance in a population of patients with moderately impaired physical function at preoperative baseline (i.e., an "indicated" population) who elect to undergo X STOP PEEK surgery.

NCT ID: NCT00480311 Terminated - Clinical trials for Lumbar Spinal Stenosis

World Health Organization Disability Assessment Schedule II (WHODAS-II) for Patients With Symptomatic Lumbar Spinal Stenosis

Start date: April 2007
Phase: N/A
Study type: Observational

The main purpose of this study is to determine the measurement characteristics of WHODAS-II (World Health Organization Disability Assessment Schedule II), as well as to analyze its correlation with symptomatic lumbar spinal stenosis (Visual Analog Scale, VAS), disability (Spanish version of the Roland Morris Questionnaire, RMQ), fear avoidance beliefs and attitudes (Spanish version of the FAB Questionnaire, FABQ), and quality of life (SF-12). Measurements will be taken at baseline and 6 days later (day 7).

NCT ID: NCT00404287 Terminated - Clinical trials for Aortic Valve Stenosis

Randomized Study to Evaluate the Efficacy of Fluvastatin on Inflammatory Markers in Patients With Aortic Stenosis.

Start date: October 1, 2006
Phase: Phase 4
Study type: Interventional

Atherosclerosis and aortic stenosis share inflammatory etiopathogenic characteristics in common. We hypothesized that statins therapy would decrease inflammatory markers concentrations in patients with degenerative aortic stenosis and halt the haemodynamic progression of the disease.

NCT ID: NCT00215059 Terminated - Clinical trials for Multivessel Pulmonary Vein Stenosis

Measurement of Angiogenic Related Growth Factors in Urine and Blood From Patients With Pulmonary Vein Stenosis

Start date: August 2000
Phase: N/A
Study type: Observational

Prospective, single center, descriptive study in 14 infants/children with multivessel pulmonary vein stenosis stratified for patients with or without underlying cardiac disease. Group 1: Patients without additional structural heart disease and multivessel pulmonary vein stenosis. Group 2: Patients with additional structural heart disease and multivessel pulmonary vein stenosis.

NCT ID: NCT00144924 Terminated - Pyloric Stenosis Clinical Trials

Open vs Laparoscopic Pyloromyotomy for Pyloric Stenosis

Start date: June 2004
Phase: N/A
Study type: Interventional

Comparison of open and laparoscopic pyloromyotomy

NCT ID: NCT00126139 Terminated - Stroke Clinical Trials

Abciximab for Prevention of Stroke Recurrence Before Endarterectomy in Symptomatic Carotid Stenosis

Start date: April 2004
Phase: Phase 3
Study type: Interventional

The purpose of the present prospective, randomized, double-blind, double dummy controlled multicenter pilot study is to investigate whether abciximab, compared with aspirin, is able to reduce the rate of recurrent ischemic strokes before and during carotid endarterectomy [CEA] (primary endpoints); and the degree of carotid stenosis, number of microembolic signal (MES) counts, number of ischemic infarcts at diffusion weighted imaging (DWI) and amount of intraluminal thrombus at pathological examination (secondary endpoints) in patients with ischemic stroke due to a >50% carotid stenosis who will undergo CEA.

NCT ID: NCT00004728 Terminated - Stroke Clinical Trials

Aspirin Or Warfarin To Prevent Stroke

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether aspirin or warfarin is more effective in preventing stroke in patients with intracranial stenosis.