Clinical Trial of Abluminus DES+ Sirolimus Eluting Stent Versus Everolimus-eluting DES

NCT ID: NCT03399994

Last Updated: 2022-07-27

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 137 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-05-21
• Study Completion Date: 2022-07-26

Brief Summary

The objective of the study is to compare angiographic and clinical performance of Abluminus DES+ versus Everolimus-eluting DES in patients with diabetes mellitus.

Detailed Description

The present clinical investigation is designed as a prospective, multicentre, national, randomized, open label, 2-arm parallel group, pilot trial comparing Abluminus DES+ versus Everolimus-eluting DES on Late Lumen Loss and clinical outcomes in diabetic patients undergoing Percutaneous Coronary Intervention.

A total of 165 patients will be recruited and randomized in the two groups in a 2:1 ratio at up to 6-8 Italian sites.

After index procedure, patients will be followed up by angiographic follow-up at 9 months and clinical follow-up at 12 months.

The study design is open label, since it is not possible to blind the investigators as to the stent type. However the members of the Event Adjudication Committee will be blinded to the patient. assignment. All medical records, source documentation and event information collected for the adjudication process will be blinded to treatment assignment.

In addition the primary endpoint will be independently evaluated by the Core-Lab which will be blinded as to group assignment.

Conditions

Coronary Artery Disease; Diabetes

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

ABLUMINUS DES+

device implantation during coronary angioplasty

Group Type: EXPERIMENTAL

device implantation during coronary angioplasty

Intervention Type: DEVICE

device implantation during coronary angioplasty

Everolimus-eluting DES

device implantation during coronary angioplasty

Group Type: ACTIVE_COMPARATOR

device implantation during coronary angioplasty

Intervention Type: DEVICE

device implantation during coronary angioplasty

Interventions

device implantation during coronary angioplasty

device implantation during coronary angioplasty

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Age>18

2. Diabetes mellitus

3. Documented CAD: stable or unstable angina, Non-ST segment MI, silent ischemia or positive functional study

4. PCI considered appropriate and feasible

5. Culprit de novo lesion in a native coronary artery with significant stenosis (>50% by visual estimate) eligible for stent implantation (no limitation on the number of treated lesions, vessel and lesion length);

6. Patient provides written informed consent

7. Patient agrees to all required follow-up procedures and visits.

8. Target lesion suitable for PCI with DES diameter between 2.5 and 4.0 mm.

Exclusion Criteria

1. The patient has a known hypersensitivity or contraindication to any of the following medications: heparin, aspirin, clopidogrel, ticlopidine, sirolimus, everolimus, and/or contrast media (patients with documented sensitivity to contrast which can be effectively pre-medicated with steroids and diphenhydramine [e.g. rash] may be enrolled. Patients with true anaphylaxis to prior contrast media, however, should not be enrolled);

2. Any contraindication to the implant of the Abluminus DES+

3. Subject is pregnant, nursing, or is a woman of child-bearing potential who is not surgically sterile, 2 years postmenopausal, or does not consistently use effective methods of contraception;;

4. History of bleeding diathesis or known coagulopathy (including heparin-induced thrombocytopenia), or will refuse blood transfusions;

5. Previous coronary intervention on target vessel in the 3-months prior to enrollment;

6. Non-cardiac co-morbid conditions with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment);

7. Patients who are actively participating in another drug or device investigational study, which have not completed the primary endpoint follow-up period;

8. Previously documented left ventricular ejection fraction (LVEF) <30%;

9. Evident cardiogenic shock before randomization;

10. Patients with left main stem stenosis (>50% by visual estimate);

11. In-stent restenosis;

12. ST-segment elevation MI;

13. Chronic total occlusion.

14. Culprit lesion to a Saphenous Vein graft

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Mediolanum Cardio Research

OTHER

Sponsor Role: collaborator

Fondazione Evidence per Attività e Ricerche Cardiovascolari ONLUS

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Antonio Colombo, MD

Role: STUDY_DIRECTOR

Ospedale San Raffaele

Azeem Latib, MD

Role: PRINCIPAL_INVESTIGATOR

Ospedale San Raffaele

Locations

Ospedale San Raffaele

Miano, Milano, Italy

Ospedale Humanitas

Rozzano, Milano, Italy

Policlinico San Donato

San Donato Milanese, Milano, Italy

Azienda Ospedaliero Universitaria Policlinico Federico II

Napoli, , Italy

Policlinico S. Matteo

Pavia, , Italy

Ospedale San Pietro, Fatebenefratelli

Roma, , Italy

Countries

Italy

Other Identifiers

ABILITY

Identifier Type: -

Identifier Source: org_study_id