Respiratory Sounds Clinical Trial
Official title:
Use of Objective Cough Counting and Breath Sounds Documenting Device, to Assess the Severity and Duration of Cough and Wheeze in Children and Adults Suffer From Acute or Chronic Respiratory Disease.
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.
Clinical background Respiratory wheezes are a characteristic symptom of asthma and other
obstructive diseases. The wheezes can be heard on the chest surface and on the trachea using
a stethoscope or by listening near the person's mouth. The wheezes are a part of the
Continuous Adventitious Breath Sounds (CABS) family, in addition to the wheezes, the rhonchi
and the whistles are also a part of this family. Each breath sound has its own unique
characteristics but all of them indicate a presence of an airway obstruction. Reducing the
obstruction by bronco dilators, for example, lowers the amount of wheezes; meaning lowers
the time period during the breathing when wheeze is present.
Cough is part of the defense mechanism to protect the lung from foreign particles and remove
secretions from the airways. However, at times it becomes a bothersome, annoying symptom
that interferes with the quality of life, sleep pattern and exercise tolerance of the
patient.
Children with respiratory infection, asthmatic children and CF patients suffer from a
multitude of pathologies of airways and are often inflicted with chronic cough.
Recently a breakthrough in continuous monitoring of respiratory symptoms was introduced. The
Wheezing Infant Monitor (WIM) is a technology that utilizes a flat coin shape microphone
that is attached to the chest and over the trachea and allows a continuous recording of the
breath sounds absorbed by the microphone. This innovative technology provides an objective
assessment of the duration, intensity and timing of the respiratory symptoms after a
computerized processing of the data.
Study background The study title is 'Use of objective cough counting and breath sounds
documenting device, to assess the severity and duration of cough and wheeze in children and
adults suffer from acute or chronic respiratory disease'. 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.
The study is an open study. Each patient will be evaluated twice during each day of
hospitalization. Each recording session will last about one hour and include 10 minutes of
pre treatment recording, administration of the treatment and continuation of the recording.
The patient will be treated according to his/her condition and the recording will not delay
the administration of the treatment in urgent cases.
The study population will consist of children with respiratory infection, asthmatic children
and CF patients who suffer from respiratory symptoms such as cough and/or shortness of
breath. The study population will include approximately 200 patients.
Patients with cough, wheeze or shortness of breath and patients (or their parents/guardians)
who gave their consent to participate in the study will be included. Subjects who are in
respiratory distress, have skin lesions precluding attachment of sensors, subject with chest
tubes and pregnant women will be excluded from the study.
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Observational Model: Case Control, Time Perspective: Prospective
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