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Assessment of Cough and Wheeze With Breath Sound Documenting Device

NCT00711399 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 55

Last updated 2010-09-14

No results posted yet for this study

Summary

The study goal is to create a database of respiratory sounds recordings, to evaluate and validate the WIM technology and to evaluate the efficacy of a specific treatment by comparing the severity of the respiratory symptoms before and after the administration of the treatment.

Conditions

  • Respiratory Sounds

Interventions

DEVICE

PulmoTrack® 2010 with WIM-PC™ and WIM-CC™ Technologies

wheeze and cough detection in hospitalized patients.

Sponsors & Collaborators

  • Carmel Medical Center

    lead OTHER

Principal Investigators

  • Yulia Goryachev, BSc · KarmelSonix Ltd.

Eligibility

Min Age
1 Year
Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-09-30
Primary Completion
2009-09-30
Completion
2010-09-30

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00711399 on ClinicalTrials.gov