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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT04319666 Not yet recruiting - Clinical trials for Coronary Artery Calcification

Intravascular Balloon Lithotripsy in Left Main Stem Percutaneous Coronary Intervention

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

The IVL Left Main study is a prospective non-randomised pilot study to investigate the mechanical and procedural outcomes and safety of distal left main stenting with coronary lithotripsy in addition to standard techniques in patients with calcific left main disease and a clinical indication for revascularisation.

NCT ID: NCT04313777 Completed - Clinical trials for Coronary Artery Disease

Virtual Reality Therapy in Cardiology

Start date: January 6, 2020
Phase: N/A
Study type: Interventional

This study evaluates the effectiveness of virtual reality (VR) therapy in the treatment of depression and anxiety symptoms in patients undergoing second stage of cardiac rehabilitation. Half of the study group will receive VR therapy (VR group) as an addition to cardiologically monitored physical training. The other half of the group (control group) will receive Schultz Autogenic Training as a standard supplement to cardiological training

NCT ID: NCT04310046 Recruiting - Clinical trials for Coronary Artery Disease

Optimal Timing of Transcatheter Aortic Valve Implantation and Percutaneous Coronary Intervention - The TAVI PCI Trial

TAVI-PCI
Start date: September 30, 2020
Phase: N/A
Study type: Interventional

The primary objective of this study is to compare, in patients with severe aortic stenosis and concomitant coronary artery disease accepted for transcatheter aortic valve implantation (TAVI) and percutaneous coronary intervention (PCI) by the multidisciplinary Heart Team, the safety and efficacy of angiography-guided complete revascularization performed after (within 1-45 days) with angiography-guided complete revascularization performed before (within 1-45 days) TAVI using the Edwards SAPIEN Transcatheter Heart Valve®.

NCT ID: NCT04308551 Not yet recruiting - Clinical trials for Stable Coronary Heart Disease

Effect of Indobufen and Aspirin on Platelet Aggregation and Long Term Prognosis in Patients With Coronary Heart Disease

Start date: December 30, 2021
Phase: N/A
Study type: Interventional

This study evaluates the effect of Indobufen and Aspirin on platelet aggregation and long term prognosis in patients with stable coronary heart disease.

NCT ID: NCT04305171 Completed - Periodontitis Clinical Trials

Effect of Non-surgical Periodontal Treatment on Cardiovascular Risk Markers

Start date: April 6, 2018
Phase:
Study type: Observational [Patient Registry]

The research question was to investigate whether non-surgical periodontal therapy could reduce cardiovascular risk markers in Coronary heart disease (CHD) patients.

NCT ID: NCT04304677 Completed - Clinical trials for Ischemic Heart Disease

Automated Algorithm Detecting Physiologic Major Stenosis and Its Relationship With Post-PCI Clinical Outcomes

Algorithm-PCI
Start date: March 22, 2016
Phase:
Study type: Observational [Patient Registry]

The presence of myocardial ischemia is the most important prognostic indicator in patients with coronary artery disease. Therefore, the purpose of percutaneous coronary intervention (PCI) is to relieve myocardial ischemia caused by the target stenosis. Fractional flow reserve (FFR) is an invasive physiologic index used to define functionally significant coronary stenosis, and its prognostic implications are supported by numerous studies. Contrary to the clear cutoff value and the benefit of FFR in pre-PCI evaluation, there have been various results regarding optimal cut-off values for post-PCI FFR. Nevertheless, the positive association between post-PCI FFR and the risk of future events has been reproduced by several studies. PCI with stent implantation is basically a local treatment and post-PCI FFR reflects both residual stenosis in the stented segment and remaining disease beyond the stented segment in the target vessel(s). Therefore, post-PCI FFR alone cannot fully discriminate the degree of contribution of each component. The relative increase of FFR with PCI is determined by the interaction of baseline severity of a target lesion, baseline disease burden of a target vessel, adequacy of PCI and residual disease burden in a target vessel. However, the most important problem in stratifying patients with better expected post-PCI physiologic results and following clinical outcome would be that there has been no clear method to identify these patients in pre-PCI phase. In this regard, we hypothesized that the amount of FFR step-up in pre-PCI pullback recording would determine the physiologic nature of target stenosis. For example, stenosis with sufficient step-up of FFR would deserve local treatment with PCI and these lesions would result in higher percent FFR increase, post-PCI FFR, and better clinical outcome than those without sufficient amount of FFR step-up. For this, we sought to develop automated algorithm to define physiologic major stenosis versus minor stenosis using pre-PCI pullback recording.

NCT ID: NCT04300764 Not yet recruiting - Obesity Clinical Trials

Gamification to Increase Mobility in the Hospital

Level Up
Start date: January 1, 2026
Phase: N/A
Study type: Interventional

Low mobility is a mediator for poor outcomes of hospital care. Wearable devices will be used and 2-way texting via patient smartphones to monitor patients' physical activity during hospitalization with and without gamification to improve patient adherence to existing guidance on recommended activity. After discharge, investigators will assess patient care utilization (SNF, inpatient vs home rehab, ED visits, readmission) and conduct validated surveys on patient function at 30 days after discharge.

NCT ID: NCT04292652 Recruiting - Clinical trials for Aortic Aneurysm, Abdominal

Myocardial Injury in Treatment of AAA

TREATROP
Start date: January 1, 2007
Phase:
Study type: Observational

Comparison of elective infrarenal aneurysm surgery with open and endovascular technique, respectively, for subclinical ischemic myocardial injury detectable with troponin T and/or 3-channel Holter ECG with ST analysis

NCT ID: NCT04290091 Active, not recruiting - Clinical trials for Coronary Artery Disease

Detection of Coronary Artery Disease With Micro Electro-Mechanical Sensors

DECADE
Start date: January 29, 2020
Phase:
Study type: Observational

This study aims to validate the sensor data of gyroscope and accelerometer in detection of hemodynamically significant CAD.

NCT ID: NCT04283734 Active, not recruiting - Clinical trials for Instantaneous Wave Free Ratio

Usefulness of the Use of Co-registration Strategy With iFR in Long and/or Diffuse Coronary Lesions

iLARDI
Start date: February 11, 2020
Phase: N/A
Study type: Interventional

Randomized controlled trial to determinate if the physiological iFR pullback evaluation with Syncvision software (intervention group) could be useful in the reduction of stent length implanted, with the potencial benefit in terms of MACEs reduction at follow-up with respect to angiographic guiding of percutaneous coronary intervention (control group).