Study to Evaluate the Safety & Performance of the Xpert(TM) Stent in Treating Below-the-knee Lesions in Patients Undergoing Percutaneous Intervention for Chronic CLI. (XCELL)

VIVA Physicians

Status and phase

Completed

Phase 1

Conditions

Peripheral Vascular Diseases

Chronic Critical Limb Ischemia

Treatments

Device: Xpert(TM) Self-expanding Transhepatic Biliary Stent System feasibility in treating chronic critical limb ischemia

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00515346

G060029

Details and patient eligibility

About

The purpose of this study is to evaluate the safety and performance of the Xpert(TM) self-expanding stent in infrapopliteal lesions as part of an overall treatment strategy in patients undergoing percutaneous intervention for the treatment of documented chronic critical limb ischemia (CLI).

Full description

Peripheral arterial disease (PAD) of the lower extremities affects roughly 25 million Americans annually. The diabetic population is particularly prone to the most severe clinical problems associated with PAD and the amputation rate amongst such patients is elevated five-fold. It has been shown that patients who undergo amputation for PAD/CLI have a much higher mortality rate in the months that follow.

Despite medical advances in the fields of pharmacology and wound care, the vast majority of patients who present with CLI will ultimately require amputation in the absence of improved blood flow. Recently, much attention has been directed towards less invasive endovascular solutions for treating patients with CLI. This study will evaluate approximately 140 subjects with Rutherford Class IV-VI PAD in a multi-center study in order to accurately estimate limb salvage rates for this treatment.

Enrollment

120 patients

Sex

All

Ages

18 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patient has documented wound care greater than or equal to 2 weeks prior to enrollment
Subject understands the duration of the study and its follow up visit requirements
Female subjects of childbearing potential have a negative pregnancy test less than 7 days before the procedure and are willing to use a reliable method of birth control for the duration of study participation
Subject has documented chronic critical limb ischemia in the target limb for two weeks with Rutherford Category 4, 5 or 6
Subject must have one of 5 approved non-invasive test results of the target limb within two weeks of enrollment.

Exclusion criteria

Life expectancy of less than 12 months
Cerebrovascular accident (CVA) or myocardial infarction (MI) within 3 months prior to enrollment
Inability to walk (with assistance is accepted)
Previous bypass surgery to target limb less than 30 days prior to study procedure
Acute thrombus at the lesion site(s)