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Coronary Disease clinical trials

View clinical trials related to Coronary Disease.

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NCT ID: NCT01510327 Completed - Clinical trials for Coronary Artery Disease

PLATINUM Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions-Pharmacokinetics (PLATINUM PK)

PLATINUM PK
Start date: October 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of the PROMUS Elementâ„¢ Everolimus-Eluting Coronary Stent System for the treatment of patients with up to 2 de novo atherosclerotic coronary artery lesions. The lesions are located in vessels that are average-sized.

NCT ID: NCT01508910 Completed - Clinical trials for Refractory Angina Pectoris

Efficacy and Safety of Targeted Intramyocardial Delivery of Auto CD34+ Stem Cells for Improving Exercise Capacity in Subjects With Refractory Angina

RENEW
Start date: April 2012
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the safety and efficacy of targeted intramyocardial delivery of Auto-CD34+ cells for increasing exercise time and amelioration of anginal symptoms in subjects with refractory angina and chronic myocardial ischemia.

NCT ID: NCT01507519 Completed - Clinical trials for Coronary Artery Disease

Study Safety and Performance of the Biomime Stent in Patients With Single, De Novo, Non-Complex Coronary Lesions

meriT-1
Start date: April 2009
Phase: N/A
Study type: Interventional

1.) Indigenously developed and designed BioMimeTM is a - predictably safe & efficacious 3rd generation drug eluting stent (DES) - with a propensity to minimize vascular injury by use of an intelligent mix of ultra-low strut thickness Co-Cr stent, - highly documented drug Sirolimus & - a biocompatible, biodegradable polymer

NCT ID: NCT01504269 Completed - Clinical trials for Coronary Artery Disease

Exercise Stress CMR Comparison Study

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

This study is being done to compare standard nuclear exercise stress testing to exercise stress magnetic resonance imaging (MRI). The investigators have successfully shown that exercise MRI works well in healthy volunteers, and the next step is to test if it works as well as nuclear stress testing in patients with known or suspected heart disease. MRIs offers superior image quality compared to echocardiography and nuclear imaging, and have the ability to image both function and perfusion. Combining the superior image quality of Cardiac MRI with the diagnostic information provided by exercise stress could result in a new, more accurate modality for diagnosing and evaluating coronary artery disease.

NCT ID: NCT01502943 Completed - Clinical trials for Coronary Heart Disease

Studies of Traditional Chinese Medicine Clinical Efficacy Evaluation Index

Start date: May 2011
Phase: Phase 4
Study type: Interventional

The purpose of the trial is to take stable angina pectoris of coronary heart disease (CHD) as examples to build a standard evaluation system for efficacy of traditional Chinese medicine (TCM). 1. Studies of evaluating reliability, validity and reactivates of Patients Report Outcomes of CHD and self-administrated scale of Stable Angina Pectoris 2. research on all indicators of CHD, and analyze their characteristics, target and function 3. theory of Invigorating Spleen to Remove Phlegm or replenish Qi, and activating blood and dissolving stasis as an example for clinical efficacy evaluation.

NCT ID: NCT01500434 Completed - Clinical trials for Coronary Artery Disease

The PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of Long De Novo Coronary Artery Lesions (PLATINUM LL)

PLATINUM LL
Start date: February 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of the PROMUS Elementâ„¢ Everolimus-Eluting Coronary Stent System for the treatment of patients with up to 2 de novo atherosclerotic coronary artery lesions. The lesions can be longer than average-sized.

NCT ID: NCT01498692 Completed - Clinical trials for Coronary Artery Disease

The PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions in Small Vessels

PLATINUM SV
Start date: February 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of the PROMUS Elementâ„¢ Everolimus-Eluting Coronary Stent System for the treatment of patients with up to 2 de novo atherosclerotic coronary artery lesions. The lesions can be located in vessels that are smaller than average-sized.

NCT ID: NCT01498003 Completed - Clinical trials for Coronary Artery Disease

Tirofiban in Stenting for Long Coronary Lesion

PETITION
Start date: November 2011
Phase: Phase 4
Study type: Interventional

Periprocedural myonecrosis or infarction are associated with short, intermediate, and long term adverse outcomes. Previous study indicated 12.6% of patients suffered a peri-procedural CK-MB rise by overlapping use of drug-eluting stents for long coronary lesions. Here the investigators hypothesize that peri-procedural use of tirofiban could reduce the occurrence of periprocedural infarciton in elective patients with long coronary lesions treated by overlapping use of drug-eluting stents.

NCT ID: NCT01496261 Completed - Clinical trials for Coronary Artery Disease

Comparative Pharmacokinetics Study of Clopidogrel and Aspirin Fixed-dose Combination Versus Separate Combination-2nd Trial

Start date: August 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to compare pharmacokinetics between fixed-dose combination and separate combination of clopidogrel 75mg/aspirin 100mg.

NCT ID: NCT01495949 Completed - Clinical trials for Coronary Artery Disease

The Cortisol Levels During Cardiac Surgery. The Comparison Between Etomidate and Thiopentone

Start date: December 2011
Phase: Phase 4
Study type: Interventional

During induction for cardiac surgery, patient hemodynamic stability is achieved by using anesthetic drugs which least affects hemodynamics such as benzodiazepines, etomidate. Etomidate although has been used for a long time but its safety regarding cortisol synthesis suppression is still doubtful. This study measures the changes in cortisol levels during cardiac surgery with the use of cardiopulmonary bypass by comparison between two inductive agents (etomidate and thiopentone). Recording data also include hemodynamic changes during induction, inotropic use for coming of cardiopulmonary bypass, blood glucose levels, amount of insulin usage, length of ICU and hospital saty.