A Randomized Prospective Multicenter Trial to Examine Vascular Healing at 1 and 6 Month(s) After Deployment of TItanium-nitride-oxide-coated OPTIMAX™ Bio-active-stent (BAS) Stent and SYNERGY™ Everolimus-Eluting Stent (EES) in Patients With Acute Coronary Syndromes by Means of Optical Coherence Tomography
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Acute Coronary Syndrome
- Sponsor
- The Hospital District of Satakunta
- Enrollment
- 110
- Locations
- 2
- Primary Endpoint
- Primary endpoint is the percentage of stent struts coverage per group
- Last Updated
- 10 years ago
Overview
Brief Summary
The purpose of this study is to compare vascular healing of the stented segment after deployment of titanium-nitride-oxide coated cobalt-chromium OPTIMAX™ bio-active stent (BAS) and SYNERGY™ everolimus-eluting stent (EES) in patients with acute coronary syndromes requiring percutaneous coronary intervention.
Patients treated with BAS will be treated with DAPT for at least 4 weeks after the procedure followed by aspirin alone, while patients in the EES group will be treated with DAPT, at least for 6 months post procedure. In addition, this study will collect initial information about the safety and effectiveness of the BAS in comparison with EES group at 30 days, 6 months, and 12 months.
Detailed Description
OPTIMAX-OCT is a prospective, randomized (1:1), study that will be conducted at 2-3 sites (Finland, Belgium) to evaluate OPTIMAX-BAS vascular healing patterns and thrombus formation with OCT at one (Study A) and six (Study B) month after stent implantation in comparison with SYNERGY-EES. Patients receiving BAS will receive dual antiplatelet treatment (DAPT) for at least four weeks followed by aspirin, while patients implanted with EES, will receive DAPT for at least 6 months followed by aspirin. Patients will be randomized to study A and B as follow: Study A: OPTIMAX-BAS (n=25) versus SYNERGY-EES (n=25). First 50 patients will be randomized to study A. OCT at 1 month follow up. Study B: OPTIMAX-BAS (n=30) versus SYNERGY-EES (n=30) Following 60 patients will be randomized to study B. OCT at 6 months follow up. Randomization is used at the time of recruitment with sealed envelopes. Patients will be randomized in 1:1 fashion. First 50 patients are randomized in study A and following 60 patients in study B. Patients in study A will have OCT follow up at 1 month after index procedure and patients in study B will have OCT at 6 months. OCT analyses will be performed blinded to patient's characteristics as well as the type of the stent used. Two (2-3) investigational sites: * Cardiovascular Center Aalst, Aalst, Belgium * Heart Center, Satakunta Central Hospital, Pori, Finland
Investigators
Pasi Karjalainen
Professor
The Hospital District of Satakunta
Eligibility Criteria
Inclusion Criteria
- •Age \>18 and \<80 years
- •STEMI or NSTEMI (assumed by investigator to be type 1 myocardial infarction, according to universal definitions of MI; EHJ 2007; 28(20):2525-38); or unstable angina (clinical symptoms of chest pain, ecg suggestive of reversible ischemia)
- •Patient is willing to comply with specified follow-up evaluations
- •Patient or legally authorized representative has been informed of the nature of the study, agrees to its provisions and has been provided written informed consent, approved by the appropriate Medical Ethics committee or Institutional Review Board.
- •Single de novo or non-stented restenosis lesion
- •Patients with two-vessel disease may have undergone successful treatment of the non-target vessel with approved devices up to and including the index procedure but must be prior to the index target vessel treatment.
- •Target lesion (maximum 20 mm length by visual estimation) to be covered by a single stent of maximum 23mm length.
- •Reference vessel diameter must be \>2.5mm and \<4.0mm by visual estimate.
- •The vessel diameter should be measured after pre-dilation procedure and after intracoronary nitroglycerin if vasospasm is suspected.
- •Target lesion \>50% and \<100% stenosed by visual estimate.
Exclusion Criteria
- •Impaired renal function (serum creatinine \>177micromol/l) or on dialysis
- •Platelet count \< 10 e5 cells/mm3
- •Patient has a history of bleeding diathesis or coagulopathy or patients in whom antiplatelet and and/or anticoagulation therapy is contraindicated.
- •Patient has received organ transplant or is on a waiting list for any organ transplant.
- •Patient has a known hypersensitivity or contraindication to aspirin, heparin/bivalirudin, clopidogrel/prasugrel/ticagrelol, cobalt chromium alloy, or contrast agent that cannot be adequately pre-medicated.
- •Patient presents with cardiogenic shock.
- •Any significant medical condition which in the Investigator's opinion may interfere with the patient's optimal participation in the study.
- •Currently participating in another investigational drug or device study.
- •Unprotected left main disease.
- •Ostial target lesions.
Outcomes
Primary Outcomes
Primary endpoint is the percentage of stent struts coverage per group
Time Frame: 6 months
In Study B, time for the OCT primary endpoint is 6 month
Secondary Outcomes
- Percentage of stent strut malapposition(1 and 6 months)
- Maximum length of segment (mm) with uncovered stent struts(1 and 6 months)
- Maximum length of segment (mm) with malapposed stent struts(1 and 6 months)
- Maximum malapposition distance(1 and 6 months)
- Total malapposition volume(1 and 6 months)
- Mean neointimal thickness(1 and 6 months)
- Percentage of protruding struts per stent(1 and 6 months)
- Stent area(1 and 6 months)
- NIH volume(1 and 6 months)
- Thrombus formation(1 and 6 months)
- In-stent late loss(6 months)
- In-segment late loss(6 months)
- In-stent binary restenosis(6 months)
- In-segment binary restenosis(6 months)
- Major adverse cardiac events defined as a composite of death, MI (Q wave or non-Q wave), emergent coronary artery bypass surgery (CABG), or justified target lesion revascularization (TLR)(1, 6, and 12 months)
- Target vessel revascularization(6 months)