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Coronary Disease clinical trials

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NCT ID: NCT05516446 Recruiting - Clinical trials for Coronary Artery Disease (CAD)

Drug Eluting Balloon Angioplasty Versus Everolimus Platinum Chrome Stent

DEBATE
Start date: August 25, 2021
Phase: N/A
Study type: Interventional

Randomized, open-label, single-center, non-inferiority clinical trial to compare late lumen loss (LLL) at 12 months in Tunisian population undergoing coronary percutaneous intervention between Drug Eluting Balloon treated group and Everolimus platinum chrome stent treated group.

NCT ID: NCT05505591 Recruiting - Clinical trials for Coronary Artery Disease

Intravenous CAngrelor in High-bleeding Risk Patients Undergoing percutaneouS Coronary Intervention (ICARUS) Registry

ICARUS
Start date: June 6, 2022
Phase:
Study type: Observational

The study will investigate the prevalence of high bleeding risk (HBR) features and will compare the clinical outcomes of HBR and non-HBR patients among those undergoing percutaneous coronary intervention and receiving cangrelor infusion.

NCT ID: NCT05502211 Recruiting - Clinical trials for Induction of General Anesthesia

A Comparison Between Ketamine-lidocaine Versus Ketamine-fentanyl for Induction on the Hemodynamic Effects in Patients With Coronary Artery Disease

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

Patients with coronary artery disease (CAD) and left ventricular systolic dysfunction (LVSD) presenting for coronary artery bypass grafting (CABG) represent a high-risk group among the cardiac surgical population. Anesthetic management of these patients is challenging due to increased risk of perioperative hypotension and subsequently increased risk of postoperative morbidity and mortality. Post induction hypotension is a modifiable risk that can be largely prevented by adjusting the technique for anesthesia induction. There is no consensus on the use of certain anesthetic induction techniques for patients CAD and left ventricular dysfunction. Anesthesia induction techniques for cardiovascular surgery are usually based on considerations such as hemodynamic stability, effects on myocardial oxygen supply, and demand and minimizing intubation stress response.To the best of our knowledge, there is no previous data comparing the efficacy of adding lidocaine versus fentanyl to the induction of anesthesia with ketamine in patients with poor ventricular function.

NCT ID: NCT05496023 Recruiting - Clinical trials for Coronary Artery Disease

Angiography-derived FFR GPS in Predicting Post-PCI Physiological and Clinical Outcomes

Angio-GPS
Start date: January 1, 2017
Phase:
Study type: Observational

To investigate the feasibility of physiological map generated from angiography-derived fractional flow reserve (FFR) (angio-FFR) pullback and its value in predicting physiological and clinical outcomes after stenting.

NCT ID: NCT05492110 Recruiting - Coronary Disease Clinical Trials

Coronary Sinus Reducer Implantation in Patients With Ischaemia and Non-obstructed Coronary Arteries and Coronary Microvascular Dysfunction.

REMEDY-PILOT
Start date: April 17, 2023
Phase: N/A
Study type: Interventional

To demonstrate the feasibility and efficacy of the CS Reducer for the treatment of patients with ischaemia and non-obstructed coronary arteries (INOCA) and coronary microvascular dysfunction (CMD) and through a nested mechanistic substudy investigate the physiological responses in the coronary microcirculation responsible for changes in myocardial perfusion.

NCT ID: NCT05489016 Recruiting - Clinical trials for Coronary Heart Disease

HuoXin Pills Intervention on Patients With Coronary Heart Disease After Drug-Coated Balloon Implantation

HAPPY-DCB
Start date: August 5, 2022
Phase: Phase 4
Study type: Interventional

This trial is a multi-center, randomized, double-blind, placebo, parallel controlled study. Objectively evaluates the curative effect of Huoxin Pills (concentrated pills) intervention on improving the prognosis of patients with coronary heart disease after drug-coated balloon implantation from a functional point of view. Huoxin Pill(concentrated pills), a traditional Chinese medicine, has been prescribed widely in the treatment of coronary heart disease, angina pectoris, and other diseases.440 patients were selected and followed up for one year. The quantitative blood flow score of the target vessel, late lumen loss, MACE incidence, and safety index were observed at 12 months.

NCT ID: NCT05474339 Recruiting - Clinical trials for Coronary Artery Disease

The Effects of Cardiac Rehabilitation on Sleep Quality and Sleep Duration in Patients After Coronary Artery Bypass Graft

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

This study aims to investigate the effects of cardiac rehabilitation on sleep quality and sleep duration in patients after coronary artery bypass graft.

NCT ID: NCT05471245 Recruiting - Coronary Restenosis Clinical Trials

AnGiographic Performance With A Sirolimus-elutiNG Balloon in the TrEatment of De Novo CoronaRy Artery Disease

GINGER
Start date: May 23, 2023
Phase: N/A
Study type: Interventional

Evaluate angiographic performance in long lesions of Sirolimus Eluting Balloon Magic Touch by Concept Medical

NCT ID: NCT05455515 Recruiting - Coronary Disease Clinical Trials

The GISE (Società Italiana di Cardiologia Interventistica) - ShockCalcium Registry

Start date: September 17, 2022
Phase:
Study type: Observational [Patient Registry]

The GISE-SHOCKCALCIUM Registry is an Investigator Driven Italian All Comers prospective, observational, multicenter Italian IVL registry of Calcified lesions Treated with Intravascular Lithotripsy. The main purpose is to evaluate the efficacy and safety of coronary lithotripsy for treatment of severe calcified lesion. A total of 2000 patients with coronary calcified lesions will be enrolled in 24 months. The registry will be conducted in approximately 50 interventional cardiology centers in Italy with at least 2 IVL procedures per 24 months. Primary endpoint: Target lesion failure (TLF) at 1 year. Secondary safety endpoints: in Hospital Target lesion failure (TLF); Target Lesion Failure at 30 days; definite or probable stent thrombosis; procedural angiographic safety endpoints. Secondary effectiveness endpoints: device crossing and IVL delivery success; angiographic success; QCA (quantitative coronary angiography) outcome; Imaging outcome.

NCT ID: NCT05442723 Recruiting - Clinical trials for CAD - Coronary Artery Disease

Extensively Diseased Left Anterior Descending Coronary Artery: On Pump vs Off Pump CABG?

Start date: February 25, 2022
Phase: N/A
Study type: Interventional

Diseased left Anterior descending coronary artery (LAD) is one of the most challenging conditions in Bypass surgery. we investigate whether on-pump coronary artery bypass grafting (CABG) is more beneficial in those critical patients or off-pump surgery.