NCT06271590Recruiting
MagicTouch™Sirolimus-Coated Balloon for Treatment of Coronary Artery Lesions in Small Vessels
The MAGICAL SV Trial - A Prospective, Multicenter, Randomized, Two-Arm, Single-blind Non Inferiority Trial to Evaluate the Safety and Efficacy of the MagicTouch™ Sirolimus-Coated Balloon in the Treatment of Small Vessels in Patients With Coronary Artery Disease.
Source: ClinicalTrials.gov · Last updated 11 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
This is a multicenter, randomized, single-blind pivotal study to evaluate the safety and efficacy of the MagicTouchTM Drug coated balloon in treatment of small vessels in patients with coronary artery disease. The objective is to establish the safety and efficacy of the Magic TouchTM Drug coated balloon in treatment of small vessels (≤2.75 mm). A total of 1605 subjects will be enrolled in a maximum of 50 study sites located in North America. Additional sites located in Europe and South America may also participate in the study, with non-US sites contributing a maximum of \~50% of enrollees.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 1605 (estimated)
- First submitted
- 13 Feb 2024
- Start date
- 20 May 2025
- Primary completion date
- Nov 2028
- Lead sponsor
- Concept Medical Inc.
- Diseases
- Coronary artery disease
- NCT number
- NCT06271590
What you commit to
- Study type: Interventional
- Planned participants: 1605
- From 20 May 2025 to the primary completion date, Nov 2028
- 24 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- Clinical Inclusion Criteria:
- Adult patient with an indication for PCI due to stable angina, NSTEACS, post-infarction angina or silent ischemia (in absence of symptoms a visually estimated target lesion diameter stenosis of ≥70%, a positive non-invasive stress test, FFR ≤0.80, or non-hyperemic pressure ratio \[NHPR\] ≤0.89 must be present)
- Subject is ≥18 and \<80 years old
- Subject is willing to comply with all protocol-required follow-up evaluations and provides written informed consent
- Angiographic Inclusion Criteria:
- Target reference vessel diameter (visual estimation) ≤2.75 mm
- Successful lesion preparation (residual stenosis \<30%), without flow-limiting complications (no or slow flow, dissection etc.)
- Target lesion(s) in a native coronary artery
- Up to two small vessel target lesions in two different vessels
- Target lesion length (visual estimation): ≥6.0 and ≤34.0 mm and can be covered by a single 40 mm balloon
- Target lesion diameter stenosis (visual estimation) \>30% and \<100% with Thrombolysis in Myocardial Infarction (TIMI) flow grade ≥2
- Clinical Exclusion Criteria:
- Planned (staged) intervention in the target vessel
- ST-segment-elevation MI within 48 hours prior to index procedure
- Subjects with acute cardiac decompensation or cardiogenic shock
- Subject with a life expectancy of less than 24 months
- Impaired renal function (glomerular filtration rate \[GFR\] \<30 mL/min)
- Documented left ventricular ejection fraction (LVEF) ≤30%
- Known allergies to acetylsalicylic acid, clopidogrel, prasugrel, ticagrelor, heparin, contrast medium, sirolimus or similar drugs (i.e., ABT-578 \[Zotarolimus\], biolimus, tacrolimus)
- Relative or absolute contraindication to dual antiplatelet therapy (DAPT) for at least 1 month (e.g., planned surgeries that cannot be delayed)
- Subject has an indication for chronic oral anticoagulation treatment and a contraindication for concomitant treatment with a P2Y12 inhibitor
- If femoral access is planned, significant peripheral arterial disease which precludes safe insertion of a 6F sheath
- Hemoglobin \<9 g/dL
- Platelet count \<100,000 cells/mm3 or \>700,000 cells/mm3
- White blood cell count \<3,000 cells/mm3
- Active infection undergoing treatment
- Clinically significant liver disease
- Cerebrovascular accident (CVA) within 3 months or has any permanent neurological defect as a result of CVA
- Subject is receiving oral or intravenous immunosuppressive therapy (e.g., inhaledsteroids are not excluded) or has known life-limiting immunosuppressive or autoimmune disease (e.g., human immunodeficiency virus, systemic lupus erythematosus, but not including diabetes mellitus)
- Subject is unlikely to comply with the follow up requirements, per investigator's assessment
- Subject currently enrolled in other investigational device or drug trial in which primary endpoint has not been reached
- Pregnant and/or breast-feeding females or females who intend to become pregnant during the time of the study
- Angiographic Exclusion Criteria:
- All exclusion criteria apply to the target lesion(s) or target vessel(s)
- Re-stenotic lesion(s), whether due to percutaneous old balloon angioplasty (POBA) or prior stenting
- True bifurcation lesion (lesion involves both main and side branch\>2.5 mm) with planned treatment of both branches per investigator assessment
- Angiographic evidence of thrombus in the target vessel
- Myocardial bridging
- Target lesion is heavily calcified
- Diffuse distal disease to target lesion with impaired runoff, TIMI flow \<2
- Non-target lesion in the target vessel requiring PCI
- Note: Non-target vessel PCI is allowed at the time of index procedure if performed prior to study intervention and if successful and uncomplicated. For target lesions located in branches of the three main vessels (left anterior descending artery \[LAD\], left circumflex artery \[LCx\], right coronary artery \[RCA\]), the term target vessel refers to the branch and not the main vessel.
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (24)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Emory University Hospital /Emory School of Medice Coordinator of this site? Confirm its status | Atlanta | United States | Not yet recruiting |
| University Hospitals, Cleveland Medical Center Coordinator of this site? Confirm its status | Brooklyn | United States | Not yet recruiting |
| Clearwater Cardiovascular and Interventional Consultants Coordinator of this site? Confirm its status | Clearwater | United States | Recruiting |
| Cleveland Clinic Coordinator of this site? Confirm its status | Cleveland | United States | Not yet recruiting |
| University Hospitals Cleveland Medical Center* Coordinator of this site? Confirm its status | Cleveland | United States | Not yet recruiting |
| Atlanta VA Medical Center Coordinator of this site? Confirm its status | Decatur | United States | Not yet recruiting |
| Dignity Health-Mercy Gilbert Medical Center Coordinator of this site? Confirm its status | Gilbert | United States | Not yet recruiting |
| University of Florida Health Sciences Center-Jacksonville Coordinator of this site? Confirm its status | Jacksonville | United States | Not yet recruiting |
| Cedars-Sinai Medical Center Coordinator of this site? Confirm its status | Los Angeles | United States | Not yet recruiting |
| North Shore University Hospital (Northwell) Coordinator of this site? Confirm its status | Manhasset | United States | Not yet recruiting |
| Loyola University Medical Center Coordinator of this site? Confirm its status | Maywood | United States | Not yet recruiting |
| West Virginia University Heart & Vascular Institute Coordinator of this site? Confirm its status | Morgantown | United States | Not yet recruiting |
| Icahn School of Medicine at Mount Sinai, Mount Sinai Hospital Coordinator of this site? Confirm its status | New York | United States | Recruiting |
| Columbia University/NYP Coordinator of this site? Confirm its status | New York | United States | Not yet recruiting |
| University of Oklahoma Health Science Center Coordinator of this site? Confirm its status | Oklahoma City | United States | Not yet recruiting |
| University of Pittsburgh Medical Center (UPMC) Coordinator of this site? Confirm its status | Pittsburgh | United States | Not yet recruiting |
| Baylor Scott & White The Heart Hospital - Plano Coordinator of this site? Confirm its status | Plano | United States | Recruiting |
| AtlantiCare Regional Medical Center Coordinator of this site? Confirm its status | Pomona | United States | Recruiting |
| Providence St. Vincent Medical Center Coordinator of this site? Confirm its status | Portland | United States | Not yet recruiting |
| NC Heart and Vascular Research, LLC Coordinator of this site? Confirm its status | Raleigh | United States | Not yet recruiting |
| Tallahassee Research Institute Coordinator of this site? Confirm its status | Tallahassee | United States | Not yet recruiting |
| Tampa General Hospital / University of South Florida Coordinator of this site? Confirm its status | Tampa | United States | Not yet recruiting |
| Montefiore Medical Center Coordinator of this site? Confirm its status | The Bronx | United States | Recruiting |
| North Mississippi Medical Center Coordinator of this site? Confirm its status | Tupelo | United States | Not yet recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.