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The Automated Fluid Shunt (AFS)in Chronic Congestive Heart Failure

Congestive Heart Failure Clinical Trial

Clinical Trial Summary

A 28-week, feasibility study to investigate the safety and efficiency of the Automatic Fluid Shunt in patients with chronic congestive heart failure, ascites and diuretic resistance.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00907673
Study type Interventional
Source NovaShunt AG
Contact
Status Completed
Phase N/A
Start date May 2009
Completion date March 2010
View Details
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