Trauma Clinical Trial - Registry AutoLog Lipid Removal & Blood Component

Status Completed

Clinical Trial Summary

The purpose of this study is to show the success of the AutoLog System in removing lipids to less than 10mg/dl in vivo. The Autolog registry has two objectives:

1. to determine the lipid removal capabilities of the Medtronic AutoLog System.

2. to obtain in vivo data on blood component removal and washing capabilities of the Medtronic AutoLog System.

Clinical Trial Description

Since the in house data strongly suggest that the Medtronic AutoLog is uniquely high performing in lipid removal in-vitro, the Registry AutoLog Lipid Removal and Blood Component Characterization is initiated to determine if the AutoLog system is successful in removing lipids in vivo as it is in-vitro. Therefore, it is expected that the lipid amounts after washing will be less than 10 mg/dl.

The study is designed as a multi-center, non-randomized, non-interventional, post market release study (a registry). The study has a single arm, without controls, as it is descriptive in nature. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Trauma

Clinical Trial Details

NCT number	NCT01565967
Study type	Observational
Source	Medtronic Cardiovascular
Contact
Status	Completed
Phase	N/A
Start date	December 2011
Completion date	March 2013

View Details

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