AirSonea Wheeze Detection Study

iSonea

Status: Unknown

Conditions: Asthma; COPD

Treatments: Device: AirSonea

Study type: Interventional

Funder types: Industry

Identifiers

NCT01927172

iS-2013-Wz

Details and patient eligibility

About

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.

Enrollment: 85 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: Single Blind

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85 participants in 1 patient group

AirSonea

Other group

Description:

Use of AirSonea to detect wheeze sounds.

Treatment:

Device: AirSonea