Coronary Artery Disease
Conditions
Brief summary
The main objective of this study is to assess the effectiveness of the CYPHER™ (sirolimus-eluting) stent in reducing in-lesion late lumen loss in de novo native coronary artery lesions in small vessels (2.25 - 2.75 mm) as compared to the small vessel tercile of the uncoated Bx VELOCITYTM Stent patients from the SIRIUS Trial, using a stenting technique that minimizes balloon trauma to the vessel and assures full coverage of the lesion with the stent.
Detailed description
This is an international, multicenter (up to 10 sites), nonrandomized, historically controlled study in patients with De Novo coronary artery lesions in small vessels treated with the CYPHER™ (sirolimus-eluting) stent as compared to the small vessel tercile uncoated Bx VELOCITYTM Stent patients from the SIRIUS Trial. A total of up to 100 patients will be enrolled in this study. Patients with de novo native coronary artery lesions \>=15mm and \<=30mm in length and \>=2.25 mm to \<=2.75 mm in diameter by visual estimation will be treated with the CYPHER™ (sirolimus-eluting) stent. Patients will be followed at 30 days, 6, 8, 9 months and at 1, 2 and 3 years post-procedure, with a repeat angiography at 8 months. In all patients Intravascular Ultrasound (IVUS) will be performed before (only in case of crossing success) and after the initial procedure. An IVUS control will also be done at 8 months follow up to assess neo-intimal growth and remodeling. This is a single lesion treatment study. Patients may have other lesions treated before the treatment of the intended lesion in the small vessel (a non-target lesion may not be located in the target vessel!). Post-procedural treatment of another lesion is only allowed after the 30-day follow-up contact has been completed or in case this is clinically needed. It is anticipated that the total length of the study will be 39 months: 3 months to complete patient enrollment and 3 years for follow-up.
Interventions
DEVICEPCI
PCI with Cypher Sirolimus-Eluting Stent
Sponsors
Cordis US Corp.
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Diagnosis of angina pectoris as defined by Canadian Cardiovascular Society Classification (CCS 1, 2, 3, 4) OR unstable angina pectoris (Braunwald Classification B&C 1-2) OR patients with documented silent ischemia; 2. Single treatment of de novo lesion in a small vessel (2.25 - 2.75 mm) in a major coronary artery in patients with single or multivessel disease. Patients with multiple lesions can be included if the other lesions are successfully treated prior to the treatment of the intended lesion in the small vessel. 3. Target vessel diameter \>=2.25 and \<=2.75mm (by visual estimation); 4. Target lesion length \>=15 and \<=30 mm.
Exclusion criteria
1. Patient has experienced a Q-wave or non-Q-wave myocardial infarction with documented total CK \>2 times normal within the preceding 24 hours or the CK and CK-MB remains above normal at the time of the treatment; 2. Has unstable angina classified as Braunwald A (1, 2, 3) or B & C 3; 3. Unprotected left main coronary disease with \>=50% stenosis; 4. Significant (\>50%) stenosis proximal or distal to the target lesion that might require revascularization or impede inflow or runoff; 5. Have an ostial target lesion; 6. Lesion \< 2.25 or \> 2.75 mm in diameter; 7. Totally occluded vessel (TIMI 0 level); 8. Documented left ventricular ejection fraction £30%; 9. Intention to treat the target lesion by direct stenting procedure.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| In-lesion late lumen loss | 8-moths post-procedure |
Countries
Switzerland
Outcome results
None listed