Dyspnea Clinical Trial
Official title:
Aerosol Inhalation Treatment for Dyspnea
The purpose of this protocol is to develop and test aerosol furosemide, as a treatment that has the potential to significantly improve symptom management and enhance the quality of care for patients with intractable dyspnea.
This is the second study in a series of studies investigating the treatment effect of
aerosolized furosemide on hospitalized patients and outpatients with intractable dyspnea. The
study will focus on patients who experience intractable dyspnea at rest or with minimal
activity, e.g., dressing, bathing, cooking, or walking stairs or short distances.
There are two parts to this study: Study 2a is a pilot study on 5-10 patients. These trials
are not blinded or placebo controlled; the investigators will use them to discover practical
problems, and take the information back to the laboratory to develop solutions. We enrolled 7
subjects for Study 2a.
Study 2b will a randomized, placebo - controlled, double- blind study on 25 - 40 patients.
The two planned treatments will be aerosolized furosemide and aerosolized saline, and will be
given to each patient on two separate days. We failed to reach our enrollment goal, and
ultimately enrolled 17 subjects for participation in Study 2b.
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