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How to Prevent Heart Failure Readmission by Using Lung Impedance Device (HOPE-HF Study) — HOPE-HF  

Heart Failure Acute Clinical Trial

Official title:
How to Prevent Heart Failure Readmission by Using Lung Impedance Device (HOPE-HF Study)

Clinical Trial Summary

The readmission of Heart Failure (HF) patients for exacerbation HF within 30-day is unmet goal. The mail reason for readmission is excessive accumulation of fluid in patient's lung. According our data (1,2) around 40% of HF patient have excessive lung fluid at discharge from HF hospitalization ("unacceptable" residual congestion on discharge). In other words, around 40% patients are discharged from HF hospitalization prematurely when they are not ready to be discharged. Only 60% of HF patients are discharged from HF admission with "acceptable" level of residual pulmonary congestion (2). There are some techniques to assess "readiness" of HF patients for discharge. Pulmonary congestion (lung fluid accumulation) may be assessed non-invasively by measurement Brain Natriuretic Peptide (BNP), (3,4), by lung ultrasound (LUS), (5-7) and by Lung Impedance (LI) method (1,2). LUS is operator depended technique. LI and BNP techniques are most reliable methods (2) and easy to use.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04080388
Study type Interventional
Source Hillel Yaffe Medical Center
Contact Michael Kleiner Shochat, MD, PhD
Phone 972-50-6246926
Email shochat1@gmail.com
Status Not yet recruiting
Phase Phase 3
Start date September 2019
Completion date September 2021
View Details
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