A Safety and Efficacy of Supralimus™ Core™ Sirolimus Eluting Stent at MAX DDHV Institute (Maximus)

Sahajanand Medical Technologies

Status

Completed

Conditions

Coronary Artery Disease

Treatments

Device: Supralimus-Core™

Device: Supralimus™ Core™ Sirolimus eluting stent

Study type

Interventional

Funder types

Industry

Identifiers

NCT00811616

The MAXIMUS study

Details and patient eligibility

About

OBJECTIVES:

The primary objective of this study is to assess the safety and efficacy of the Supralimus - Core™ Sirolimus Eluting Stent in de novo native vessel obstructive coronary artery disease.

STUDY DESIGN:

This is a single centre, prospective study. Approximately 105 patients were enrolled in the study. Patients were followed for twelve months post-procedure. All patients were to have a repeat angiography at 8 months.

STUDY POPULATION:

The study population consisted of approximately 105 patients with de novo native vessel obstructive coronary artery disease with no specific criteria. Patients from the daily practice were included. Patients had to meet all eligibility criteria for inclusion into the study.

ENDPOINTS:

The primary safety endpoint of the study is defined as Major Adverse Cardiac Events (MACE) at 30 days.

The primary efficacy endpoint is the in-stent binary restenosis rate at 8-month follow-up determined by off-line Quantitative Coronary Angiography.

The following secondary efficacy endpoints were assessed

Angiographic success
Procedure success
Quantitative Coronary Angiography derived vessel parameters in-stent and 5 mm proximal and 5 mm distal from the edge of the stent: acute gain, MLD, % DS, late loss, mean diameter. In-stent pre-, post and at 8-month follow-up.
Clinically justified Target Lesion Revascularization (TLR) at 12 months

The following secondary safety endpoints were assessed:

MACE until 12 months
Device related SAEs until 12 months
Angiographic stent thrombosis: Subacute (after procedure until 30 days) and Late (after 30 days until 12 months)

Enrollment

105 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

The patient must be >= 18 years of age;
Symptomatic ischemic heart disease (CCS class 1 -4 , Braunwald class IB, IC, IIB, IIC, IIIB,IIIC) and/or objective evidence of myocardial ischemia;
Vessel size of >= 2.5 and <= 3.5mm.
Target lesions which can be covered by stent in a manner lesion stent ratio of at least 1.5.
Acceptable candidate for coronary artery bypass surgery (CABG);
Target lesion stenosis is >50% and <100% (TIMI flow I) (visual estimate);
The patient has been informed of the nature of the study agrees to its provisions and has provided written informed consent, approved by the appropriate Medical Ethics Committee (MEC) or Institutional Review Board (IRB).

Exclusion criteria

Women of childbearing potential;
Impaired renal function (creatinine > 2.0 mg/dl or 177 µmol/l);
Any patient who has a platelet count < 100,000 cells/mm3 or > 700,000 cells/mm3, a WBC of < 3,000 cells/mm3, or documented or suspected liver disease (including laboratory evidence of hepatitis);
Recipient of heart transplant;
Restenotic or lesion in graft.
Patient with a life expectancy less than 12 months;
Known allergies to aspirin, clopidogrel bisulphate (Plavix), ticlopidine (Ticlid), heparin or stainless steel;
Any significant medical condition which in the investigator's opinion may interfere with the patient's optimal participation in the study;
Currently participating in an investigational drug or another device study, or subject to inclusion in another investigational drug or another device study during follow-up.

Angiographic Exclusion criteria:

Unprotected left main coronary artery disease with >=50% stenosis;
Angiographic evidence of thrombus (thrombus larger than half the diameter of the vessel and/or requiring other interventions such as angiojet, exciser, thrombolysis, etc.);
Ejection fraction <= 30%;