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Comparing PA Compliance During and After Decompensation in HFP

Congestive Heart Failure Clinical Trial

Official title:
Comparison of Noninvasive Pulmonary Artery Compliance During and After Decompensation in Heart Failure Patients

Clinical Trial Summary

Pulmonary Artery Compliance measurements will be obtained with the Respirix device in patients with congestive heart failure decompensation. Echocardiogram, weight measurements, and BNP will also be gathered as independent measures of decompensation in the clinic. Pulmonary Artery Compliance measurements will be made daily during the hospital stay. Patients can continue using the device at home for the next 3 weeks. Each patient will serve as their own control and relative changes from their baseline will be recorded for each parameter.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03914222
Study type Interventional
Source Theranova, L.L.C.
Contact Megan Nolte
Phone 4159268616
Email mnolte@theranova.com
Status Recruiting
Phase N/A
Start date June 24, 2019
Completion date February 2020
View Details
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