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Clinical Trial Summary

The purpose of this protocol is to develop and test optimal delivery of aerosol furosemide, a treatment that has the potential to significantly improve symptom management and enhance the quality of care for patients with intractable dyspnea.


Clinical Trial Description

This is study of aerosol treatment in a laboratory model of dyspnea in healthy subjects. This study is the first in a series of studies that will include investigation of a second dose in the laboratory and investigation of the treatment effect in hospitalized patients with refractory dyspnea. The outcome of this first study will determine the details of protocol for the succeeding studies. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01440764
Study type Interventional
Source Beth Israel Deaconess Medical Center
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date September 2011
Completion date August 2017

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