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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT01394705 Completed - Clinical trials for Coronary Artery Disease Risk High

FITT Exercise Counseling With Interactive Accelerometry and Physical Activity in Adolescents at Increased Risk of Early Cardiovascular Disease: A Pilot Study

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

This pilot study seeks to compare the change in energy expenditure and fitness levels of patients seen in the Children's Hospital Preventive Cardiology program receiving standard of care provider exercise counseling to similar patients receiving Frequency, Intensity, Time, Type (FITT) exercise prescription and counseling combined with BodyMedia supported by an online interactive tool. The investigators primary hypothesis is that this interactive technology coupled with support from a exercise specialist will increase the energy expenditure of the investigators patients over standard of care provider counseling. The investigators Secondary hypotheses include greater improvement in measured physical fitness Peak oxygen consumption (VO2max), oxygen consumption (VO2) at anaerobic threshold (AT) and ventilation/carbon dioxide (VE/VCO2) slope, lipid profiles, blood pressure, arterial stiffness, body mass index (BMI), BMI percentile, and self-efficacy in the intervention group compared to control.

NCT ID: NCT01393028 Terminated - Chest Pain Clinical Trials

Computed Tomography Versus Exercise Testing in Suspected Coronary Artery Disease

CRESCENT
Start date: July 2011
Phase: N/A
Study type: Interventional

Direct non-invasive coronary imaging by computed tomography (CT) has the potential to improve the workup of patients with stable chest pain complaints. The objective of the study is to compare in a randomized fashion the effectiveness and efficiency of a CT angiographic driven workup of suspected coronary artery disease in comparison to the standard workup using stress testing.

NCT ID: NCT01392846 Completed - Clinical trials for Coronary Artery Disease

The IRIS-Resolute Integrity (IRIS-Integrity)

Start date: July 2011
Phase:
Study type: Observational

This is a prospective, observational, cohort study to evaluate the relative efficacy and safety of Resolute Integrity stent compared to other (drug eluting stents) DES.

NCT ID: NCT01390155 Completed - Clinical trials for Coronary Artery Disease

Characterization of Ischemia Related Changes in Esophageal Electrocardiography

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

Esophageal electrocardiography (eECG) has important advantages compared to standard ECG recordings. Coronary artery disease leading to myocardial ischemia is very common and has potentially severe consequences for patients. To date, the investigators don't know the influence of ischemia on the eECG. The goal of the present study is to assess ischemic changes of the eECG induced by balloon occlusion of coronary arteries in patients undergoing coronary angiography.

NCT ID: NCT01389375 Completed - Clinical trials for Coronary Artery Disease

Instrumental Sealing of Arterial Puncture Site Closure Device Versus Manual Compression Trial

ISAR-CLOSURE
Start date: July 2011
Phase: Phase 4
Study type: Interventional

Are novel vascular closure devices noninferior to manual compression regarding access site complications after coronary angiography?

NCT ID: NCT01388660 Recruiting - Clinical trials for Coronary Artery Disease

Pharmacokinetic Assessment of Simultaneous Administration of Clopidogrel and Aspirin

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

This is a randomized, open-label, single-dose, two-sequence, two-period crossover study to investigate the pharmacokinetics between a tablet containing 75 mg of Clopidogrel and 100 mg of Aspirin and the simultaneous administration of the separate formulations of the two drugs in healthy male volunteers.

NCT ID: NCT01386021 Completed - Clinical trials for Coronary Artery Disease

Saphenous Vein Allografts for Coronary Bypass

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

The primary objective of this observational study is to evaluate the function (patency) of cryopreserved saphenous vein allografts used as coronary artery bypass grafts (CABG) for patients with occlusive coronary artery disease.

NCT ID: NCT01385319 Active, not recruiting - Clinical trials for Coronary Artery Disease

Zotarolimus-eluting Endeavor Sprint Stent in Uncertain DES Candidates (ZEUS) Study

ZEUS
Start date: June 2011
Phase: Phase 3
Study type: Interventional

To prospectively evaluate in a multicenter open label trial whether the use of zotarolimus-eluting ENDEAVOR Stent implantation in patients at low restenosis or at high bleeding or thrombotic risk will decrease the incidence of 12-month major adverse cardiac events (MACE) including overall death, any myocardial infarction (MI) or any target vessel revascularization (TVR).

NCT ID: NCT01384747 Terminated - Clinical trials for Coronary Artery Disease

Effect of Fimasartan for Modification of Atheroma Vulnerability in DEFERred Coronary Disease (FIMA-DEFER)

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

- Fimasartan will be more beneficial in stabilizing the plaque vulnerability compared to control group in deferred coronary lesions. - Fimasartan will be more beneficial in reducing total plaque volume compared to control group in deferred coronary lesions. - Fimasartan will be more beneficial in reducing functional impairment of stenotic lesions (assessed by FFR:Fractional Flow Reserve) in deferred coronary lesions.

NCT ID: NCT01384721 Recruiting - Clinical trials for Coronary Artery Disease

Computed Tomography Coronary Angiography (CTCA) Prognostic Registry for Coronary Artery Disease

PRORECAD
Start date: September 2010
Phase:
Study type: Observational

The study aims at pooling a large population of patients with suspected coronary artery disease (CAD) who underwent Computed Tomography Coronary Angiography (CTCA) and who were adequately stratified in the first place. Then the investigators will be able to assess the incremental value of CTCA in the stratification of prevalence of disease (non obstructive/obstructive) and prognosis of patients with suspected CAD). The added information to current evidence is how reliable and to what extent CTCA can define the actual burden of disease and cardiovascular risk.