NCT00992966

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

20
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial recruitment is currently suspended
Enrollment
80

participants targeted

Target at P50-P75 for all trials

Status
suspended

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

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 9, 2009

Completed
Last Updated

August 20, 2010

Status Verified

August 1, 2010

First QC Date

October 8, 2009

Last Update Submit

August 19, 2010

Conditions

Keywords

to acquire database of pneumonia cases in children

Eligibility Criteria

Age3 Years - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodProbability Sample
Study Population

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

MeSH Terms

Conditions

Pneumonia

Condition Hierarchy (Ancestors)

Respiratory Tract InfectionsInfectionsLung DiseasesRespiratory Tract Diseases

Study Officials

  • Liora Kornreich, M.D

    Shnider medical center

    PRINCIPAL INVESTIGATOR
  • Liora Kornreich, Professor

    Shnider medical center

    PRINCIPAL INVESTIGATOR

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