Anatomical and Perioperative Predisposing Factor for Limb Occlusion of Incraft Infrarenal Endograft (LIMIT Study)

IRCCS San Raffaele400 enrolled

Overview

The aim was to determine, within the patient enrolled in three controlled prospective studies, INNOVATION, INSPIRATION and INSIGHT (Sponsor: Cordis, A Cardinal Health Company) studies which are preoperative and postoperative anatomical risk factors associated to limb occlusion. In the three studies the total number of enrolled patients was 400, of whom 134 enrolled in the US

Study Type

OBSERVATIONAL

Enrollment

400

Conditions

Aneurysm Abdominal

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients with abdominal aortic aneurysm, who have been treated with the INCRAFT® Grafting System (AAA Stent-Graft System). * All cases treated with Incraft who were enrolled in three controlled prospective studies, INNOVATION, INSPIRATION and INSIGHT (Sponsor: Cordis, A Cardinal Health Company) Exclusion Criteria: * no exclusion criteria

Locations (1)

IRCCS Ospedale San Raffaele

Milan, Italy

Outcomes

Primary Outcomes

limb occlusion

freedom from limb occlusion

Time frame: 30 days

freedom from death

survival

Time frame: 30 days

Data from ClinicalTrials.gov

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