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UnknownNCT01206621

Vibration Response Imaging (VRI) in Dyspnea Patients Presenting to the ED

Assessment of the Utility of Vibration Response Imaging (VRI) in Evaluating Dyspnea Patients Presenting to the Emergency Department

Status
Unknown
Phase
Study type
Observational
Enrollment
530 (estimated)
Sponsor
Deep Breeze · Industry
Sex
All
Age
41 Years
Healthy volunteers
Not accepted

Summary

For the patient with acute dyspnea in the ED, early differentiation between CHF and non-CHF causes is essential for proper management. The capacity to triage patients quickly and accurately has a beneficial impact upon outcome, disposition, stratification and length of stay in the ED and required length of hospital admission. The ability to assess pulmonary status rapidly by quantitative regional vibration technology offers significant potential advantage for earlier diagnosis. The VRI technique may provide a quick and accurate method of differentiating between dyspnea due to HF and dyspnea due to pulmonary causes; thereby improving management and outcomes.

Conditions

Timeline

Start date
2010-08-01
Primary completion
2011-06-01
Completion
2011-06-01
First posted
2010-09-22
Last updated
2011-05-13

Locations

8 sites across 2 countries: United States, Israel

Source: ClinicalTrials.gov record NCT01206621. Inclusion in this directory is not an endorsement.

Vibration Response Imaging (VRI) in Dyspnea Patients Presenting to the ED (NCT01206621) · Clinical Trials Directory