Modification of Coronary Calcium With Laser Based Intravascular Lithotripsy for Coronary Artery Disease (FRACTURE)
Condition(s) studied
Investigational drug(s) / intervention(s)
Intravascular lithotripsy: Lithotripsy-enhanced percutaneous coronary intervention of de novo, calcified, stenotic coronary artery lesions prior to stenting.
Study summary
The FRACTURE Trial is a prospective, non-randomized, single-arm, multicenter, interventional study in US and international centers.
Eligibility
Primary outcome measure(s)
- Primary Safety Endpoint — Within 30 days following procedure
Freedom from major adverse cardiac events (MACE) within 30 days following the index procedure. - Primary Effectiveness Endpoint — Immediately after the intervention/procedure/surgery
Procedural success defined as successful stent delivery with a final residual stenosis \<50% (assessed by angiographic core laboratory) and freedom from in-hospital MACE.
Trial sites (46)
| Facility | City | Region | Status |
|---|---|---|---|
| Scripps Health | La Jolla | California | |
| Cedars-Sinai Heart Institute | Los Angeles | California | |
| Riverside Community Hospital | Riverside | California | |
| Southern California Permanente Medical Gp. / Kaiser Permanente | San Diego | California | |
| Los Robles Hospital & Medical Center | Thousand Oaks | California | |
| Medical Center of the Rockies | Loveland | Colorado | |
| Nova Clinical Research Centers/Manatee Memorial Hospital | Bradenton | Florida | |
| The Cardiac & Vascular Institute | Gainesville | Florida | |
| HCA FL Memorial Hospital | Jacksonville | Florida | |
| HCA Florida Largo Hospital | Largo | Florida | |
| Northeast Georgia Medical Center | Gainesville | Georgia | |
| Wellstar Research Institute | Hiram | Georgia | |
| Brigham and Women's Hospital | Boston | Massachusetts | |
| Massachusetts General Hospital | Boston | Massachusetts | |
| Trinity Health Michigan Heart | Ypsilanti | Michigan | |
| Metropolitan Heart and Vascular Institute | Coon Rapids | Minnesota | |
| North Mississippi Medical Center | Tupelo | Mississippi | |
| Saint Luke's Hospital of Kansas City | Kansas City | Missouri | |
| The Valley Hospital | Paramus | New Jersey | |
| New York-Presbyterian/Brooklyn Methodist Hospital | Brooklyn | New York | |
| The Icahn School of Medicine at Mt. Sinai | New York | New York | |
| Nyph/Cuimc | New York | New York | |
| Montefiore Medical Center | The Bronx | New York | |
| NC Heart and Vascular Research | Raleigh | North Carolina | |
| Providence Heart Institute | Portland | Oregon | |
| Wellspan York Hospital | York | Pennsylvania | |
| Tristar Centennial Medical Center | Nashville | Tennessee | |
| Austin Heart Research | Austin | Texas | |
| Methodist Healthcare Methodist Research Institute | San Antonio | Texas | |
| Intermountain Health | Murray | Utah | |
| Chippenham Johnson Willis Hospital | Richmond | Virginia | |
| Onze-Lieve-Vrouwziekenhuis, afgekort OLV ziekenhuis | Aalst | Belgium | |
| Aarhus University Hospital | Aarhus | Denmark | |
| Segeberger Kliniken GmbH, | Bad Segeberg | Germany | |
| Cellitinnen Krankenhaus St. Vinzenz | Cologne | Germany | |
| SJG St. Paulus GmbH, St.-Johannes-Hospital Dortmund | Dortmund | Germany | |
| Klaipeda University Hospital | Klaipėda | Lithuania | |
| Vilnius University Hospital Santaros Klinikos | Vilnius | Lithuania | |
| Amsterdam University Medical Center | Amsterdam | Netherlands | |
| Erasmus Medical Center | Rotterdam | Netherlands |
+ 6 more sites — see the full list on the official registry below.
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06181240 on ClinicalTrials.gov ↗ ← All trials in the UK