Sprinter Legend Balloon Catheter

Medtronic

Status

Completed

Conditions

Coronary Artery Disease

Treatments

Procedure: Percutaneous Coronary Intervention

Device: Sprinter Legend 1.25mm Balloon Catheter

Study type

Interventional

Funder types

Industry

Identifiers

NCT00961311

IP-111

Details and patient eligibility

About

Open label, single-arm trial to study the safety and effectiveness of the Sprinter Legend 1.25 mm angioplasty balloon.

Full description

The study examines acute outcomes when the Sprinter Legend 1.25mm balloon catheter is used for enlarging coronary luminal diameters during PCI procedures.

Enrollment

51 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patient is greater than18 years of age and able to give informed consent.
Patient with stenotic lesions in coronary arteries or bypass graft stenosis that are suitable for percutaneous coronary intervention (PCI).
The patient has single or multiple vessel coronary artery disease and clinical evidence of ischemic heart disease, stable or unstable angina, silent ischemia, and/or a positive functional study.
Female patients of childbearing potential must have a negative pregnancy test within seven (7) days before the procedure.
Patient or patient's legal representative has been informed of the nature of the trial and agrees to its provisions and has provided written informed consent as approved by the Institutional Review Board (IRB) of the respective investigational site.
Patients with symptomatic ischemic heart disease due to stenotic lesions in coronary arteries or bypass graft stenosis that are amenable to percutaneous treatment.

Exclusion criteria

A known hypersensitivity or contraindication to aspirin, heparin, or bivalirudin, anti-platelet medications, or sensitivity to contrast media, which cannot be adequately pre-medicated.
A serum creatinine level > 2.0 mg/dl within seven days prior to index procedure.
Evidence of an acute myocardial infarction within 72 hours of the intended index procedure (defined as: Q wave myocardial infarction or non-Q wave myocardial infarction having creatine kinase myocardial-band isoenzyme (CK-MB) or troponin elevated above the Institution's upper limit of normal).
During the index procedure, the target lesion requires additional treatment with a cutting balloon, any artherectomy, any laser, thrombectomy, etc.
History of stroke or transient ischemic attack (TIA) within the prior 6 months.
Active peptic ulcer or upper gastrointestinal (GI) bleeding within the prior 6 months.
History of bleeding diathesis or coagulopathy or will refuse blood transfusions.