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Stenosis clinical trials

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NCT ID: NCT01873586 Completed - Stenosis Clinical Trials

OsteoStrux™ Collagen Ceramic Scaffold in Instrumented Lumbar Spine Fusion

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

The objective of this study is to prospectively evaluate the performance of Integra's OsteoStrux Collagen Ceramic Scaffold combined with bone marrow aspirate as an adjunct for instrumented posterolateral spine fusion, as compared to local autograft.

NCT ID: NCT01742117 Completed - Clinical trials for Coronary Artery Disease

Tailored Antiplatelet Therapy Following PCI

TAILOR-PCI
Start date: May 2013
Phase: Phase 4
Study type: Interventional

Clopidogrel is an anti-platelet medication approved by the U.S. Federal Drug Administration (FDA) for use in patients who undergo Percutaneous Coronary Intervention (PCI) with coronary stent implantation. Anti-platelet medications work to prevent blood clots from forming. Some studies have suggested that patients who have a certain genetic liver enzyme abnormality (known as cytochrome P450 2C19 [CYP2C19] *2 or *3 allele) may have a reduced ability to activate clopidogrel, and therefore may have a lowered response to clopidogrel. It is thought that perhaps people who have a coronary stent procedure may have this genetic liver enzyme abnormality. There is a research genetic test available to determine whether or not someone has this genetic liver enzyme abnormality. Ticagrelor, is a newer anti-platelet drug that is not dependent on the CYP2C19 liver enzyme for its activation and hence in poor clopidogrel metabolizers, alternative drugs like Ticagrelor have been recommended for use as an anti-platelet agent after PCI. The purpose of this study is to determine if genetic testing can identify the best anti-platelet therapy, for patients who undergo a coronary stent placement and do not activate clopidogrel very well.

NCT ID: NCT01714804 Completed - Stenosis Clinical Trials

Efficacy and Safety of Integra Accell Evo3 DBM in Instrumented Lumbar Spine Fusion

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

The objective of this study is to prospectively evaluate the performance of Integra Accell Evo3 Demineralized Bone Matrix as an adjunct for instrumented lumbar spine fusion with a retrospective comparison to a historical patient cohort.

NCT ID: NCT01620320 Withdrawn - Stenosis Clinical Trials

Stress Echocardiography Versus Coronary Angiography for Left Main Stenosis Detection

ESTRIE-TC
Start date: July 2010
Phase: N/A
Study type: Observational

Left main stenosis use to be treated by bypass but with the improvement of angioplasty techniques, an increasing number of patients are submit to left main coronary angioplasty. Consequences of left main intra stent stenosis can be disastrous yet, for the moment, no precise recommendation concerning the follow up of these patients exist. The investigators ought to determine if stress echocardiography can predict left main intra stent stenosis as well (non inferiorly)as control angiography that use to be done.

NCT ID: NCT01617538 Recruiting - Stenosis Clinical Trials

Application of Contrast Enhance Ultrasound to Evaluate Hemodynamics Change in MCA With Moderate to Severe Stenosis

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

Objective: To monitor and evaluate the change of intracranial hemodynamics and MCA stenosis after 24-week atorvastatin treatment using CEUS, CTA and DSA. Study design: Total 30 patients (60 arteries) will be enrolled in this study, who had MCA infarction within 6 months prior to screening, and has not received any statins treatment before stroke. Eligible patient will receive atorvastatin 40mg treatment for 24 weeks. Hemodynamics changes and MCA stenosis will be evaluated using CEUS at baseline, 3-month,and 6-month. MCA stenosis, bloodstream velocity, as well as clinical symptoms will be assessed at each visit and compared to baseline.

NCT ID: NCT01430299 Completed - Stenosis Clinical Trials

Efficacy and Safety of Accell Evo3 Demineralized Bone Matrix (DBM) in Instrumented Posterolateral Lumbar Spine Fusion

Start date: June 2011
Phase: N/A
Study type: Interventional

The objective of this study is to prospectively evaluate the performance of Integra Accell Evo3 Demineralized Bone Matrix as an adjunct for posterolateral spine fusion with a retrospective comparison to a historical patient cohort.

NCT ID: NCT01381952 Completed - Aneurysm Clinical Trials

Image Quality and Radiation Dose in Angiography

Start date: June 2011
Phase: N/A
Study type: Interventional

ClarityIQ is a novel X-ray imaging technology, that combines advanced real-time image noise reduction algorithms, with state-of-the-art hardware to reduce patient entrance dose significantly. This is realized by anatomy-specific optimization of the full acquisition chain (grid switch, beam filtering, pulse width, spot size, detector and image processing engine) for every clinical task individually. Furthermore, smaller focal spot sizes and shorter pulses are used, which are known to positively influence image quality . The final effect on the clinical image quality is investigated in this study.

NCT ID: NCT01123850 Terminated - Spondylolisthesis Clinical Trials

CopiOs Posterolateral Fusion Procedure

Start date: June 2010
Phase: Phase 2
Study type: Interventional

To compare radiographic data collection from patients undergoing instrumented PLF with CopiOs(R) BVF or instrumented PLF with autologous bone and to assess overall clinical outcomes. Patients will serve as self controls.

NCT ID: NCT00912561 Terminated - Stenosis Clinical Trials

Effects of Intense Aerobic Exercise on the Cerebrovascular Reserve Capacity in Patients With Hemodynamically Relevant Intra- and Extracranial Stenoses

Exercise
Start date: June 2009
Phase: N/A
Study type: Interventional

The purpose of this trial is to study the improvement of cerebral hemodynamics in high risk stroke patients with impaired Cerebrovascular Reserve (CVR) due to high grade stenosis of the internal carotid (ICA) or middle cerebral artery (MCA) by Intense Aerobic Exercise (IAEx).

NCT ID: NCT00691314 Completed - Stroke Clinical Trials

Efficacy and Safety of Stent Implantation in Symptomatic Extra- and Intracranial Artery Stenosis

ESSCAS
Start date: June 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of stent implantation in patients with symptomatic extra- and intracranial artery stenosis and to determine its role in secondary prevention of ischemic stroke.