Clinical Trials Directory

Trials / Unknown

UnknownNCT04080388

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

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Hillel Yaffe Medical Center · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTLung Impedance DeviceThe non-invasive lung impedance device enables assessment of the level of pulmonary congestion and can be an indication for additional anti-congestive treatment.
DRUGAnti-congestive treatmentContinuation of in-hospital anti-congestive treatment

Timeline

Start date
2019-09-01
Primary completion
2021-09-01
Completion
2021-09-01
First posted
2019-09-06
Last updated
2019-09-06

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT04080388. Inclusion in this directory is not an endorsement.