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Constriction, Pathologic clinical trials

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NCT ID: NCT00904254 Not yet recruiting - Carotid Stenosis Clinical Trials

The Use of Anti-CD4 mAb-Fragment for Imaging of Local Inflammation in Patients With Carotid Artery Stenosis

Start date: January 2015
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to proof the concept of EP 1645 as a diagnostic tool for carotid artery atherosclerosis and plaque instability and to assess the safety and tolerability of this diagnostic agent, a monoclonal antibody fragment (Fab') conjugated with the diagnostic radionuclide 99mTc. Safety and tolerability will be determined by adverse events (AEs) observed and reported upon administration of the product and the absorbed dose of radiation.

NCT ID: NCT00892632 Terminated - Biliary Stricture Clinical Trials

Confocal Endomicroscopy for Biliary Strictures -Phase I

Start date: April 2009
Phase: N/A
Study type: Interventional

The investigators hypothesize that the confocal endomicroscopy imaging of the biliary strictures during ERCP will differentiate between benign and malignant strictures in vivo and has increased sensitivity compared to biliary brushing/biopsy, and that direct cholangioscopic guidance of pCLE is more accurate than fluoroscopic guidance.

NCT ID: NCT00891527 Completed - Clinical trials for Pulmonary Veno Occlusive Disease

Pilot Study Using Avastin and Gleevec to Treat the Progression of Intraluminal Pulmonary Vein Stenosis

PVS
Start date: October 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The objective of this study is to conduct a pilot study using biologic agents Avastin and Gleevec to treat progression of multivessel intraluminal pulmonary vein stenosis in children.

NCT ID: NCT00887744 Completed - Spinal Stenosis Clinical Trials

Intermittent Neurogenic Claudication Treatment With APERIUS®

INCA
Start date: November 2006
Phase: Phase 4
Study type: Interventional

The primary purpose of the study is to measure the change in severity of symptoms and ability to function in every day activities in patients suffering from degenerative lumbar spinal stenosis after treatment with the Aperius® device.

NCT ID: NCT00885768 Completed - Clinical trials for Renal Artery Stenosis

Prevalence of Renal Artery Stenosis in Patients Referred for Cardiac Catheterization

RAS
Start date: July 2008
Phase: Phase 3
Study type: Observational

All patients referred for coronary angiography will simultaneously be evaluated for renal artery stenosis and then stenosis more than 50% will be analyzed according to clinical conditions, risk factors and lab data.

NCT ID: NCT00883571 Completed - Anal Stenosis Clinical Trials

Comparative Study of the House Advancement Flap, Rhomboid Flap, and Y-V Anoplasty

Start date: April 2002
Phase: N/A
Study type: Interventional

This prospective randomized study included 60 consecutive patients suffering from anal stenosis in the period from April 2002 to December 2008. They admitted to colorectal surgery unit, Mansoura university hospital, Egypt. According to the classification proposed by Milson and Mazier(5), all patients had moderate to severe anal stenosis. There were 43 males and 17 female with a mean age 34 + 5.2 years ranging from 18 up to 63 years.

NCT ID: NCT00817102 Completed - Clinical trials for Coronary Artery Stenosis

Validation of Stenosis Assessment by Coronary Artery Computed Tomography Against Invasive Measurements of Fractional Flow Reserve in Patients With Significant Coronary Artery Stenoses

Start date: November 2008
Phase: N/A
Study type: Interventional

This study will evaluate the effectiveness of CorCTA by comparing the results of the test with another imaging method called Fractional Flow Reserve (FFR), which is done as a part of the cardiac catheterization.

NCT ID: NCT00811330 Recruiting - Clinical trials for Aortic Valve Stenosis

Effects of High Dose Atorvastatin in Patients With Surgical Aortic Stenosis

Start date: December 2008
Phase: Phase 3
Study type: Interventional

The purpose of the study is to see if statin therapy will optimize myocardial response to cardiopulmonary bypass during aortic valve replacement (AVR) for aortic valve stenosis (AVS) (Phase I) and optimize left ventricular reverse remodeling following AVR (Phase II). Preliminary evidence indicates that perioperative statin therapy reduce mortality and morbidity following cardiac surgery. Pleiotropic effects of statins may induce myocardial preconditioning and optimize myocardial and systemic responses to cardiopulmonary bypass during AVR. Furthermore statin therapy after AVR may contribute to an optimal left ventricular reverse remodeling.

NCT ID: NCT00805311 Terminated - Stroke Clinical Trials

Aggressive Medical Treatment Evaluation for Asymptomatic Carotid Artery Stenosis

AMTEC
Start date: April 2009
Phase: Phase 4
Study type: Interventional

The aim of this study is to determine whether optimal medical treatment can postpone carotid endarterectomy.

NCT ID: NCT00805051 Completed - Bleeding Clinical Trials

Acquired Von Willebrand Syndrome in Severe Aortic Stenosis

Start date: October 2008
Phase: N/A
Study type: Observational

Patients with severe aortic stenosis often suffer from an acquired Von Willebrand syndrome by degeneration of the polymers during passage through the narrow valve leading to turbulences. We hypothesized that the diagnosis of acquired von Willebrand syndrome influence perioperative blood loss in patients undergoing open cardiac valve replacement.