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Percutaneous Coronary Intervention Clinical Trials

Reviewed by TrialFinderData Editorial Team · Updated

6 recruiting trials for Percutaneous Coronary Intervention. Eligibility criteria explained in plain English.

TrialFinderData lists 6 Percutaneous Coronary Intervention clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.

Across the trials that carry a phase, Phase 4 is the largest group at 67% (2 studies); the largest phase groups are Phase 4: 2, Phase 2 / Phase 3: 1.

Research is led by VA Office of Research and Development (1), National Institute of Cardiology, Warsaw, Poland (1), Federico II University (1), among the most active sponsors registered for these trials.

The most frequently studied intervention is Remote ischemic preconditioning (device, 1 trial), followed by Sham remote ischemic conditioning, PCI.

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.
6
Total Trials
6
Recruiting Now
0
Phase 3 Trials
6
Sponsors

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Recruiting Trials

Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.

RECRUITINGPhase 2 / Phase 3NCT04982419

Remote Ischemic Preconditioning for Renal and Cardiac Protection in Congestive Heart Failure (RICH) Trial

This is a prospective, double-blind, sham-controlled, multicenter, randomized clinical trial is to study the effects of remote ischemic preconditioning on contrast-associated...

Sponsor: VA Office of Research and DevelopmentEnrolling: 2403 locations
RECRUITINGNCT07330622

Polish Registry of Percutaneous Coronary Intervention for Chronic Total Occlusions

The goal of this observational study is to evaluate the safety, efficacy, and clinical outcomes of percutaneous coronary intervention (PCI) for chronic total occlusions (CTO) in...

Sponsor: National Institute of Cardiology, Warsaw, PolandEnrolling: 100020 locations
RECRUITINGNCT05248165

Naples PCI Registry

The aim of the Naples PCI registry is to collect prospective data on baseline clinical, laboratory, and angiographic characteristics of patients undergoing PCI for acute or...

Sponsor: Federico II UniversityEnrolling: 50001 location
RECRUITINGPhase 4NCT05638867

NOAC Therapy Guided by PARIS Risk Score and D-dimer in Patients With ACS After PCI

The goal of this clinical trial is to compare short-term Triple Antithrombotic Therapy (DAPT + Rivaroxaban) followed by DAPT with standard DAPT in selected ACS patients with high...

Sponsor: China National Center for Cardiovascular DiseasesEnrolling: 39441 location
RECRUITINGNCT06101862

Coronary Computed Tomography Versus Invasive Angiography for Non-ST Elevation Acute Coronary Syndrome

Coronary computed tomography angiography (CCTA) is a widely accepted initial diagnostic test for individuals suspected of having chronic coronary syndromes. However, there is...

Sponsor: Rigshospitalet, DenmarkEnrolling: 23006 locations
RECRUITINGPhase 4NCT06909565

Inclisiran Versus Placebo for the Prevention of Major Adverse Cardiovascular and Limb Events in Patients Undergoing...

V-INTERVENTION will evaluate the effectiveness of inclisiran in preventing major cardiovascular and limb events in patients receiving percutaneous coronary or peripheral arterial...

Sponsor: Duke UniversityEnrolling: 600020 locations

Frequently Asked Questions

There are currently 6 clinical trials for Percutaneous Coronary Intervention, with 6 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.

To join a clinical trial for Percutaneous Coronary Intervention, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.

Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for Percutaneous Coronary Intervention, representing treatments closest to potential FDA approval.

Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.

Sources: ClinicalTrials.gov, FDA
Last updated:

Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.