Study Stopped
Study initiation has been delayed due to Sponsor decision
Vibration Response Imaging (VRI) in Children With Acute Respiratory Symptoms
1 other identifier
observational
80
0 countries
N/A
Brief Summary
The VRI device may provide a complementary diagnostic tool for lung examination and aid the physician in determining whether a chest x-ray should be performed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 8, 2009
CompletedFirst Posted
Study publicly available on registry
October 9, 2009
CompletedAugust 20, 2010
August 1, 2010
October 8, 2009
August 19, 2010
Conditions
Keywords
Eligibility Criteria
A total number of 80 patients in the age range of 3-18 and consisting of both boys and girls, preferably in an equal distribution
You may qualify if:
- Subject's parent or legal guardian, is able and willing to read the Informed Consent, understands the Informed Consent, and provides written Informed Consent for the subject; if the minor child is in fact able to give consent, the minor's consent must be obtained in addition to the consent of the minor's legal guardian.
- Boy or girl in the age range of 3-18 years.
- Patient presented with acute respiratory complaints, acute cough, onset of shortness of breath, or fever.
- Patient referred by ED physician and presented for CXR.
You may not qualify if:
- Body habitus or skin condition that might prevent the placement of the sound sensors on the back (e.g. severe scoliosis, kyphosis, chest wall deformation, skin lesion on the back or compression fracture);
- Potentially contagious skin lesion on the back;
- Subject has had lung surgery;
- Subject was prescribed the CXR for monitoring or follow up of a lung condition that pre-existed the current, acute symptoms.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Deep Breezelead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Liora Kornreich, M.D
Shnider medical center
- PRINCIPAL INVESTIGATOR
Liora Kornreich, Professor
Shnider medical center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
October 8, 2009
First Posted
October 9, 2009
Last Updated
August 20, 2010
Record last verified: 2010-08