Percutaneous Coronary Intervention (PCI) Clinical Trials

Clinical trials related to Percutaneous Coronary Intervention (PCI) Procedure

A Prospective, Multicenter, Randomized Controlled Trial to Investigate the Value of Coronary CT Angiography in the Understanding and Management of Coronary Calcium

Status: Recruiting
Location: See all (13) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The OPTIMAL randomized clinical trial has been designed to compare two imaging strategies and to test the hypothesis that a calcium modification strategy informed by coronary CT angiography (CCTA) will improve procedural efficiency and effectiveness compared with the current standard of care (IVUS-guided PCI) while achieving similar clinical outcomes in patients with hemodynamically significant calcified coronary artery disease.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• The subject must be at least 18 years of age and younger than 85 years old

• Subject must have evidence of myocardial ischemia (e.g., stable angina, silent ischemia (ischemia in the absence of chest pain or other anginal equivalents), unstable angina, or acute myocardial infarction) suitable for PCI. Patients with a clinical indication for revascularization presenting with stable coronary artery disease or stabilized acute coronary syndrome defined as follows unstable angina (Braunwald class IB, IC, IIB, IIC, IIIB, IIIC), patients with NSTEMI without high-risk features such as recurrence of chest pain, ST-segment depression\>1mm in ≥6 leads plus STsegment elevation in aVR, life-threatening arrhythmias, mechanical complications of MI, resuscitated cardiac arrest, GRACE risk score\>140.

• All target vessels must have reference vessel diameter (visually assessed by CCTA) ≥ 2.5 mm

• Subject must provide written informed consent before any study-related procedure

Locations
United States
Massachusetts
Bringham and Women's Hospital
NOT_YET_RECRUITING
Boston
Minnesota
Minneapolis Heart Institute
NOT_YET_RECRUITING
Minneapolis
New Jersey
HACKENSACK MERIDIAN HEALTH, Inc
NOT_YET_RECRUITING
Jersey City
New York
Columbia University Irving Medical Center/NewYork-Presbyterian Hospital
NOT_YET_RECRUITING
New York
Weill Medical College of Cornell University
NOT_YET_RECRUITING
New York
Other Locations
Spain
Hospital Universitari Vall Hebron
RECRUITING
Barcelona
Hospital Universitario de Leon
RECRUITING
León
Hospital Universitario La Paz
RECRUITING
Madrid
United Kingdom
University Hospitals of Leicester NHS Trust
NOT_YET_RECRUITING
Leicester
St Bartholomew's Hospital (Barts Health NHS Trust)
NOT_YET_RECRUITING
London
St George's University Hospitals NHS Foundations Trust
NOT_YET_RECRUITING
London
Newcastle Hospitals NHS Foundations Trust
NOT_YET_RECRUITING
Newcastle
John Radcliffe Hospital, Oxford
NOT_YET_RECRUITING
Oxford
Contact Information
Primary
CAROLINA FOCELLA
cfocella@crf.org
001 917 753 6695
Backup
CARLOS COLLET, MD,PhD
carloscollet@gmail.com
001 917 753 6695
Time Frame
Start Date: 2025-12-22
Estimated Completion Date: 2030-01-01
Participants
Target number of participants: 700
Treatments
Experimental: CT-guide calcium modification strategy
Pre-procedural CT will be used to determine lesion characteristics.
Active_comparator: IVUS-guide calcium modification strategy
Pre-procedural IVUS will be used to determine lesion characteristics.
Sponsors
Leads: Fundación EPIC

This content was sourced from clinicaltrials.gov