Clinical Trials Logo

Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

Filter by:

NCT ID: NCT02628288 Not yet recruiting - Clinical trials for Coronary Artery Disease

COmplex Bifurcation PCI: AXXESS Device + Absorb BVS, vs Modified T Stenting With Absorb BVS

COBRAII
Start date: December 2015
Phase: N/A
Study type: Interventional

Comparison of healing responses after treatment of complex bifurcation lesions with a dedicated bifurcation device (Axxess™ Biolimus Eluting Coronary Bifurcation Stent System + Absorb BVS in the distal branches) versus the Modified T stenting technique using Absorb BVS: an optical coherence tomography (OCT) analysis.

NCT ID: NCT02628002 Completed - Clinical trials for Coronary Artery Disease

Anti-gravity Treadmill Exercise in Stress Myocardial Perfusion Imaging

Start date: December 2015
Phase: N/A
Study type: Interventional

This study will test the hypothesis that the anti-gravity treadmill can be safely used in stress nuclear myocardial perfusion imaging in patients unable to perform conventional treadmill exercise. This will be foundational evidence on which to consider a larger clinical trial to show that the anti-gravity treadmill improves diagnostic specificity across all cardiovascular stress testing modalities including treadmill-alone, exercise stress echocardiogram, exercise SPECT as well as having implications for cardiac PET and MRI in the future.

NCT ID: NCT02627521 Recruiting - Clinical trials for Coronary Artery Disease

Optimizing Timing of CABG in Patients Presenting With ACS and Treated With Ticagrelor

CABG-TIME
Start date: July 2015
Phase: Phase 4
Study type: Interventional

The administration of Ticagrelor have demonstrated superiority to Clopidogrel in patients presenting with acute coronary syndrome (ACS) and remains a first line therapy as an adjunct to aspirin for patients admitted with ACS. The patient population treated with Ticagrelor at an early time point includes non ST elevation myocardial (NSTEMI) patients and those undergoing primary angioplasty for ST elevation myocardial infarction (STEMI). It is estimated that 10-15% of patients presenting with ACS have advanced coronary artery disease requiring Coronary Artery Bypass Surgery (CABG). The treatment guidelines recommend a delay of 5-7 days for CABG surgery in these patients for normalization of Ticagrelor induced platelet inhibition to reduce the risk of peri-operative bleeding. This delay may expose these high risk patients to adverse cardiac events while waiting for Ticagrelor effect to wean off. Furthermore, this empirical application of 5-7 day delay in all patients may be unnecessary due to the significant inter individual variability in response to Ticagrelor. There is limited data to determine the optimum timing of CABG surgery in ACS patients treated with Ticagrelor. The present study will determine the optimum timing of CABG in ACS patients treated with a loading and/or maintenance dose of Ticagrelor.

NCT ID: NCT02626806 Recruiting - Clinical trials for Coronary Artery Disease

Exercise-induced High-sensitivity Troponin Levels as a Predictor for Obstructive Coronary Artery Disease

EUROCAD
Start date: November 2013
Phase: N/A
Study type: Observational

1. To compare hs-TnT levels after a cardiac stress test in patients with vs. patients without CAD 2. To assess the level of post-exercise hs-TnT predicting CAD (using ROC-analysis) 3. To determine the sensitivity, specificity and accuracy of this exercise-induced hsTopT level in predicting CAD, either alone or in relation to traditional patient-related and exercise test-related metrics

NCT ID: NCT02625493 Completed - Clinical trials for Coronary Artery Disease

Patient Preference for Radial Versus Femoral Vascular Access

PREVAS
Start date: June 2014
Phase: N/A
Study type: Observational

The purpose of this study is to determine the preference of patients regarding the vascular access site in future coronary procedures. We hypothesize that patients prefer the lesser invasive procedure via radial access.

NCT ID: NCT02624297 Recruiting - Clinical trials for Coronary Artery Disease (CAD)

Chemoreflex Control of Sympathetic Activity in Patients With Coronary Artery Disease

Start date: January 2014
Phase: N/A
Study type: Interventional

The investigators hypothesize that chemoreflex response of muscle sympathetic nerve activity (MSNA) during hypoxia and hypercapnia will be increased in coronary artery disease (CAD) patients and that the presence of obstructive sleep apnea (OSA) will potentiate these responses. And, that the exercise training would decrease the chemoreflex response of MSNA in these patients.

NCT ID: NCT02624180 Completed - Clinical trials for Coronary Artery Disease

Inflammatory Pathogenesis of Coronary Atherosclerosis in HIV

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

The investigators are studying whether an anti-inflammatory intervention improves impaired coronary endothelial function (CEF) in HIV+ people with no clinical coronary artery disease (CAD).

NCT ID: NCT02623140 Active, not recruiting - Clinical trials for Ischaemic Heart Disease

BIOFREEDOM Stent Versus ORSIRO Stent: SORT OUT IX

SORT OUT IX
Start date: December 2015
Phase: Phase 4
Study type: Interventional

The aim of the Danish Organization for Randomized Trials with Clinical Outcome (SORT OUT) is to compare the safety and efficacy of the polymer-free Biolimus-eluting BIOFREEDOM stent with a biodegradable-polymer Sirolimus-eluting ORSIRO stent in a population-based setting, using registry detection of clinically driven events

NCT ID: NCT02622100 Terminated - Clinical trials for Coronary Artery Disease

Evaluation of Effectiveness and Safety of Bioresorbable Vascular Scaffold in Routine Clinical Practice

IRIS BVS
Start date: February 26, 2016
Phase:
Study type: Observational

The purpose of this study is to evaluate the relative effectiveness and safety of Bioresorbable Vascular Scaffold compared to other (drug eluting stents) DES.

NCT ID: NCT02621216 Recruiting - Clinical trials for Coronary Heart Disease

Tilburg Health Outcomes Registry of Emotional Stress in Coronary Intervention

THORESCI
Start date: December 4, 2013
Phase:
Study type: Observational [Patient Registry]

Background of the study: Percutaneous coronary interventions (PCI) have become mainstay treatment for acute coronary artery disease and the number of patients receiving PCI is vastly growing. However, relatively little long-term follow-up studies of large real-world clinical samples exist that have looked at the real-world effects of PCI treatment and adherence to current guidelines. Psychological risk factors are important in determining prognosis after PCI, and undergoing PCI may increase the risk of low mood. To date, studies have examined single psychological risk factors, without taking into account their relatedness. Moreover, guidelines are advocating psychosocial screening in early cardiovascular disease, but the screening test as proposed in the prevention guideline has not yet been validated or tested. Although the detrimental effects of psychological risk factors on cardiovascular prognosis are known, the mechanisms through which they exert these effects are yet unclear. It is to be expected that not one but multiple biological (inflammation, endothelial dysfunction) and behavioural (coping styles, poor self-care, consultation behaviour) pathophysiological processes play a role, and that these processes interact with each other. In PCI patients the mechanisms linking psychological risk to poor prognosis are still to be investigated. Objective of the study: 1. To examine the adherence to the prevention and PCI guidelines and the effects thereof on long term prognosis in PCI patients. 2. To evaluate the effectiveness of the psychosocial screening instrument of the European Society of Cardiology Prevention guideline 2012. 3. To examine effects of clustering psychological risk factors on several networks of potentially mediating mechanisms and long term outcomes in a large sample of PCI patients.