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Safety Study of a Selective Cytopheretic Device (SCD) in Patients With Acute Renal Failure

Acute Renal Failure Clinical Trial

Official title:
A Multi-Center Pilot Study to Assess the Safety and Efficacy of A Selective Cytopheretic Device (SCD) Treatments In Patients With Acute Renal Failure (ARF)

Clinical Trial Summary

The purpose of this protocol is to evaluate the safety of a selective cytopheretic device (SCD) in patients that are on continuous renal replacement therapy (CRRT) for acute renal failure (ARF).

Clinical Trial Description

Acute renal failure is a condition where the kidneys are not capable of producing adequate urine. Therefore, another way to remove waste from the body is needed to hopefully allow time for the kidneys to heal. One method of removing waste from the body is called Continuous Renal Replacement Therapy (CRRT) or variations of that therapy. This study will evaluate the safety of the device while it is connected to the CRRT tubing for up to 7 days. Patients will be followed up until day 60 following the treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01072682
Study type Interventional
Source SeaStar Medical
Contact
Status Completed
Phase N/A
Start date February 2010
Completion date May 2011
View Details
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