Post Marketing Surveillance of the CentrosFLO™ Tunneled IJ Catheter
NCT ID: NCT02349308
Last Updated: 2015-09-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
10 participants
OBSERVATIONAL
2013-10-31
2015-07-31
Brief Summary
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Detailed Description
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The main difference of the CentrosFLO catheter is in the design of the tip. Current "split tip" catheters have two free ends that diverge, but are each essentially straight segments. In the CentrosFLO catheter the arterial lumen bends in an arc back towards the venous lumen, and the venous lumen bends towards the arterial lumen. As a result, the catheter has two curved surfaces that will rest against the vena cava wall to automatically "center" the catheter within the vein. The contact points of the catheter against the vena cava wall should be smaller and more disperse than with current straight-tip or split catheters. The following drawing demonstrates the design of the catheter, showing the current recommendation that the arterial port always be to the left.
The goal of the study is to demonstrate the stability of blood flow with the CentrosFLO catheter, during intermittent dialysis over a period of 6 months after placement. The investigators plan to enroll 10 patients in the study.
Conditions
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Study Design
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PROSPECTIVE
Study Groups
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CentrosFLO Long Term Hemodialysis Catheter
Schedule placement of catheter. Arterial tip of the catheter should be placed at or just above the junction of the right atrium and superior vena cava, with the arterial lumen on the left side of the catheter. The venous limb will extend into the right atrium. Catheter will be locked with the usual heparin lock solution for a newly placed catheter (at least 500 units per lumen). Fluoroscopic images will document tip position.
CentrosFLO Long Term Hemodialysis Catheter
Interventions
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CentrosFLO Long Term Hemodialysis Catheter
Eligibility Criteria
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Inclusion Criteria
* The patients may have had a prior tunneled catheter for dialysis in the right IJ site.
* Patients will be expected to need use of the catheter for more than 45 days
Exclusion Criteria
* Patients unable to give informed consent
ALL
No
Sponsors
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Merit Medical Systems, Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Steven Ash
Role: PRINCIPAL_INVESTIGATOR
Consulting Physican
Locations
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Angiocare
Tucson, Arizona, United States
Arrowhead Regional Medical Center
Colton, California, United States
Olive View- UCLA Medical Center
Los Angeles, California, United States
IU School of Medicine
Indianapolis, Indiana, United States
IU Health Arnett
Lafayette, Indiana, United States
Sierra Nephrology
Reno, Nevada, United States
OSU Medical Center
Columbus, Ohio, United States
Countries
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Other Identifiers
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2013224
Identifier Type: -
Identifier Source: org_study_id
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