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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT01638078 Not yet recruiting - Clinical trials for Coronary Artery Disease

Thalidomide fOr the Prevention of Restenosis After Coronary ArtERy Stent Implantation

TOP RACER
Start date: January 2014
Phase: Phase 4
Study type: Interventional

Percutaneous coronary intervention (PCI) with the use of bare metal stents is associated with restenosis in approximately 10% to 50% of cases. Stenting may induce endothelial damage/dysfunction and inflammatory reactions, which in turn delay healing and endothelialization and may lead to restenosis and atherosclerosis within the stented segments. The sedative and antinausea drug thalidomide has been shown to have both anti-inflammatory and antioncogenic properties that could be of benefit in case of PCI with stenting.

NCT ID: NCT01637896 Terminated - Myocardial Ischemia Clinical Trials

A Comparison Between Paclitaxel-eluting Balloon in Combination With BMS Implantation vs Conventional Balloon and DES Implantation

ELICOPTER
Start date: June 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy of predilation with paclitaxel-eluting balloon and bare metal stent implantation VS conventional balloon and drug-eluting stent implantation in terms of restenosis

NCT ID: NCT01637012 Completed - Clinical trials for Myocardial Infarction

Prospective, Single-arm, Multicenter Study for Evaluation the Safety and Effectiveness of the ALEX Stent in a Real-world Setting of Percutaneous Coronary Interventions in Patients With Coronary Heart Disease

ALEX OCT
Start date: February 2012
Phase: Phase 4
Study type: Interventional

To evaluate the safety and effectiveness of the ALEX stent in a real-world setting of percutaneous coronary interventions in patients with coronary heart disease.

NCT ID: NCT01636271 Completed - Clinical trials for Coronary Heart Disease

SB-480848 in Major Adverse Cardiovascular Events - Integrated Summary of Efficacy and Safety From the STABILITY Trial (LPL100601) and the SOLID-TIMI-52 Trial (SB-480848/033)

Start date: October 2011
Phase: N/A
Study type: Observational

The overall objective of this integrated analysis is to evaluate the clinical safety and efficacy of long-term treatment with darapladib enteric coated tablets, 160mg, as compared to placebo when added to standard of care in subjects with clinical manifestations of cardiovascular disease (chronic coronary heart disease (CHD) and post Acute Coronary Syndrome (ACS)). With respect to efficacy, the key purpose of this integrated analysis is to evaluate the effects of darapladib on the following endpoints: urgent coronary revascularization for myoacrdial ischemia, fatal/non-fatal stroke, time to subsequent Major Adverse Cardiovascular Event (MACE), and heart failure requiring hospitalization. The first occurrent of MACE, Major and total coronary events as well as the individual components of MACE will also be evaluated descriptively.

NCT ID: NCT01635881 Completed - Clinical trials for Coronary Artery Disease

Evaluation of Coronary Luminal Diameter Enlargement With Emergeā„¢ 1.20 mm PTCA Dilatation Catheter

Start date: July 2012
Phase: Phase 3
Study type: Interventional

To evaluate the acute safety and device procedural success of the Emerge 1.20 mm PTCA dilatation catheter when used as a pre-dilatation device in the stenotic portion of coronary arteries or bypass grafts.

NCT ID: NCT01633359 Not yet recruiting - Clinical trials for Coronary Artery Disease

The Association Between Very Small Embryonic-like Stem Cells and the Prognosis of Coronary Artery Disease Patients

VSEL-CAD
Start date: July 2012
Phase: Phase 4
Study type: Interventional

Hypothesis: Peripheral blood Very Small Embryonic-like Stem Cells (VSELs) are different in coronary artery disease (CAD) patients from those without CAD, which might account for the benefits of Atorvastatin in CAD patients.

NCT ID: NCT01632670 Completed - Clinical trials for Coronary Artery Disease

Functional Change in Endothelium After Cardiac cAtheterization, With and Without Music Therapy

FEAT
Start date: June 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of music therapy before, during, and after cardiac catheterization is associated on (a) change in reactive hyperemia index measured before and after catheterization using peripheral arterial tonometry and (b) patient stress and discomfort measured by a questionnaire, as compared to the standard of care (no music during cardiac catheterization). The hypothesis of the study is that music therapy during cardiac catheterization will be associated with more favorable change in reactive hyperemia and higher patient satisfaction compared to no music playback.

NCT ID: NCT01632501 Completed - Clinical trials for Coronary Heart Disease

Safety and Efficacy of the Percutaneous Intervention Performed With Devices of a Single-brand

Tsunami
Start date: January 2011
Phase: N/A
Study type: Interventional

The freedom of choice in medicine is based on the physician's ability to treat their patients with the best available therapy. The armamentarium for percutaneous intervention is frequently determined on the basis of subjective criteria and the experience of the interventional cardiologist. The evaluation of devices used in coronary intervention, especially angiography and its clinical outcomes, has rarely been investigated; the exceptions are studies on stents. Therefore, the freedom of choice for the interventional cardiologist has been challenged, especially because of cost restrictions. This way this study aims to assess the safety and efficacy of a device of a single brand in performing percutaneous transluminal coronary angioplasty (guide catheters, guidewires, balloons, and stents) in selected patients.

NCT ID: NCT01631409 Withdrawn - Clinical trials for Coronary Heart Disease (CHD)

Estimation of the Long Term Effectiveness of Routine Use of Cardiac Shock Wave Therapy

CSWTSPB40
Start date: September 2013
Phase: N/A
Study type: Observational

This study is dedicated to determination of the long term effectiveness of coronary heart disease (CHD) treatments - cardiac shock wave therapy (CSWT) in comparison with other kinds of medical and surgical treatment. For that purpose the investigators will observe the patients with CHD who enrolled in this study in their routine course of treatment. But the investigators will not interfere with the patient treatment. Each participant will be followed-up for five years. The collected data will allow to determine if the particular method, CSWT, could really make any additional contribution to the more traditional methods of CHD treatment and if the CSWT is only temporarily effective or could exert the long term effect as well.

NCT ID: NCT01628562 Completed - Hypertension Clinical Trials

A Comparison of the Perioperative Hemodynamic Effects of Remifentanil and Esmolol in Intracranial Surgery

Start date: June 2012
Phase: Phase 4
Study type: Interventional

It was hypothesized that the use of esmolol as an alternative to remifentanil with sevoflurane inhalation anesthesia during intracranial surgery, could provide better hemodynamic conditions and cause lesser side effects in the perioperative period. It was the main objective of this study to compare the effect of esmolol and remifentanil on the incidence of tachycardia and hypertension and the intraoperative fentanyl consumption. The comparison of postoperative troponine I and creatine phosphokinase levels and EKG changes were the secondary objectives.