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Clinical Research Directory

Browse clinical research sites, groups, and studies.

8 clinical studies listed.

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Coronary Artery Disease(CAD)

Tundra lists 8 Coronary Artery Disease(CAD) clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT06843005

Serial Coronary CTA-based Plaque Progression Detection for Management of Coronary Heart Disease

The primary objective of this study is to evaluate whether a management strategy based on coronary computed tomography angiography (CCTA) for patients with non-obstructive coronary artery disease can improve the LDL-C target achievement rate compared to a traditional management strategy without follow-up CCTA, thereby reducing the incidence of major adverse cardiovascular and cerebrovascular events over a 3 years period, including all-cause mortality, myocardial infarction, ischemia driven revascularation and stroke.

Gender: All

Ages: 18 Years - 80 Years

Updated: 2026-03-24

1 state

Major Adverse Cardiovascular Events (MACE)
Prevention
Coronary Artery Disease(CAD)
+1
RECRUITING

NCT07439133

Comparison of Diagnostic Accuracy Between XTR004 PET MPI and the Composite Index of Quantitative Coronary Angiography (QCA) and Fractional Flow Reserve (FFR)

The primary objective of this study is to evaluate the effectiveness of visual reading in XTR004 PET myocardial perfusion imaging (MPI) for detecting restrictive stenosis, using quantitative coronary angiography (QCA) and fractional flow reserve (FFR) as reference standards in patients with suspected or known coronary artery disease.

Gender: All

Ages: 18 Years - 80 Years

Updated: 2026-03-03

Coronary Artery Disease(CAD)
RECRUITING

NCT07386418

Study of Lesion-Specific Invasive Haemodynamic Angina Thresholds

ORBITA-SOLAR is an invasive physiological cardiac catheterisation study that aims to determine whether different coronary stenoses have different angina thresholds. The angina threshold is defined as the amount of coronary flow reduction required to reproduce symptoms. Sixty patients with symptoms of stable angina and 2 coronary artery stenoses amenable to percutaneous coronary intervention (PCI) will be recruited. This study will use intra-coronary balloon inflation during supine exercise on an ergometer to measure the fractional flow reserve (FFR) and non-hyperemic pressure ratio (NHPR) that relates to angina onset, in real time, at the location of each stenosis.

Gender: All

Ages: 18 Years - Any

Updated: 2026-02-18

Angina (Stable)
Ischaemic Heart Desease
Coronary Artery Disease(CAD)
NOT YET RECRUITING

NCT07306728

Effect of Femoral Region Ice Bag Application on Patients' Clinical Outcomes Post-Percutaneous Coronary Intervention

Coronary artery disease (CAD) remains a leading cause of morbidity and mortality worldwide, necessitating advancements in diagnostic techniques (Parulkar et al., 2025). According to the British Heart Foundation, over 250 million individuals worldwide are living with CAD, making it the most commonly diagnosed heart condition globally. In 2021, CAD was responsible for approximately 9 million deaths, accounting for about one in every seven deaths globally

Gender: All

Ages: 18 Years - Any

Updated: 2025-12-29

Coronary Artery Disease(CAD)
Percutaneous Coronary Intervention
RECRUITING

NCT07163858

Postural Mobilization Compared to Noradrenaline Only in Off-Pump CABG Surgery

This interventional prospective randomized study is designed to compare hemodynamic management using postural mobilization (+/- noradrenaline) versus noradrenaline only in patients undergoing open-heart coronary artery bypass graft (CABG) surgery.

Gender: All

Ages: 18 Years - Any

Updated: 2025-12-03

1 state

Coronary Artery Disease With Need for Bypass Surgery
Coronary Artery Disease(CAD)
Coronary Artery Bypass
+5
NOT YET RECRUITING

NCT07162792

The Safety and Efficacy of New-Generation BRS vs. DCB for De Novo Large Coronary Artery Lesions: A Prospective RCT

This study plans to enroll 150 patients who are candidates for "intervention without implantation" therapy and they will be randomly assigned in a 1:1 ratio to either the new-generation Firesorb scaffold group (BRS group, N=75) or the drug-coated balloon group (DCB group, N=75). All enrolled patients will undergo angiographic follow-up at 1 year post-procedure, and serial follow-up (via telephone or outpatient visit) will be performed at 1 month, 6 months, 1 year, 2 years, 3 years, 4 years, and 5 years post-procedure. The primary study endpoint was percentage diameter stenosis at 1 year post-procedure.

Gender: All

Ages: 18 Years - 80 Years

Updated: 2025-09-09

Coronary Artery Disease(CAD)
de Novo Coronary Lesions
ENROLLING BY INVITATION

NCT07158307

Safety and Efficacy of GENOSS® DCB With a Shellac Plus Vitamin E Excipient in Patients With De Novo Lesion

The GENOSS PCB-De Novo study aims to evaluate the long-term efficacy and safety of a paclitaxel-coated balloon catheter containing shellac and vitamin E excipients (Genoss® DCB) in patients with De novo small coronary artery disease.

Gender: All

Ages: 19 Years - Any

Updated: 2025-09-05

Coronary Artery Disease(CAD)
RECRUITING

NCT07107568

Assessment of Coronary Artery Disease Before Transcatheter Aortic Valve Replacement: A Randomized, Multicenter, Non-Inferiority Trial

The goal of this clinical trial is to determine whether a non-invasive coronary assessment strategy using photon-counting detector computed tomography (PCD-CT) is non-inferior to invasive coronary angiography (ICA) for evaluating coronary artery disease (CAD) prior to transcatheter aortic valve replacement (TAVR) in patients with severe aortic stenosis.

Gender: All

Ages: 18 Years - Any

Updated: 2025-08-22

Aortic Valve Stenosis and Insufficiency
Coronary Artery Disease(CAD)
Transcatheter Aortic Valve Replacement (TAVR)