COPD | AirSonea Wheeze Detection Study
COPD research study
What is the primary objective of this study?
The purpose of this study is to determine if the AirSonea device provides an objective assessment of breath sounds for the presence of wheeze in both medical and home environments.
Who is eligible to participate?
Inclusion Criteria: - Part I: Participants presenting to an Acute Care Setting with an exacerbation of asthma or chronic obstructive pulmonary disease symptoms - Part II: Volunteer participants without asthma - Part III: Participants with asthma - For all parts of study - Age: 18 years or older - Participant has signed an Informed Consent after having the Study explained to them. Exclusion Criteria: - Any medical finding by the physician that would exclude the patient from participating. - < than 18 years of age
Which medical condition, disease, disorder, syndrome, illness, or injury is researched?
Interventions can include giving participants drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available or noninvasive approaches such as surveys, education, and interviews.
Research studies and clinical trials typically have two or more research arms. An arm is a group of people who receive the same treatment in the study.
AirSoneaUse of AirSonea to detect wheeze sounds.
Start Date: September 2013
Primary Outcome: Device Efficacy
Secondary Outcome: Wheeze Rate break points
Study sponsors, principal investigator, and references
Lead Sponsor: iSonea