An All-Comers Observational Study of the MicroStent™ Peripheral Vascular Stent System in Subjects With Peripheral Arterial Disease

Ki vehet részt

• Any subject with below the knee, at the ankle level or below the ankle peripheral arterial lesions previously treated or intended to be treated with the MicroStent® System per the current indications for use
• For across the ankle joint intervention, distal runoff to digital branches or arcuate arteries must be present on angiography prior to MicroStent deployment
• Subject's age is ≥ 18 years
• Subject must be willing to sign a patient informed consent form

Ki nem vehet részt

• Subject has a known allergy to concomitant medication, contrast agents (that cannot be medically managed), anti-platelet, anti-coagulant or thrombolytic medications
• Subject is pregnant or planning to become pregnant during the study duration
• Subject has a life expectancy of less than one (1) year
• Subject is enrolled in another study that has not reached its primary endpoint at the time of enrollment