Safety and Performance Evaluation of the Nephronyx System for the Treatment of Patients With ADHF

Recruiting N/A Interventional Study
Acute Decompensated Heart Failure
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
10 (estimated)
Sponsor
Nephronyx LTD · Industry
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About This Trial

The objective of this interventional study is to evaluate the safety and functional performance of the Nephronyx System in patients with ADHF, presenting clinical signs of volume overload and compromised response to diuretics.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patient admitted to the hospital with a primary diagnosis of ADHF * Patient has signs of volume overload as evidence by a score of ≥ 4 on the EVEREST score * Patient with Left Ventricular Ejection Fraction LVEF \>15% * Patient has compromised response to diuretics * NT-proBNP …
Contacts

Sagy Karavany

972-8-9999734

sagy@nephronyx.com

CONTACT