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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04873882
Other study ID # 21550
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 16, 2019
Est. completion date August 27, 2021

Study information

Verified date April 2021
Source University of Virginia
Contact Allison J Bechtel, MD
Phone 434.924.2283
Email as4sk@hscmail.mcc.virginia
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

With the aid of computerized sound analysis, digital acoustic monitoring could provide a more sensitive, specific, and quantifiable indicator for perioperative respiratory abnormalities including wheezing. It is probable that the digital stethoscope has utility in the detection, monitoring, and resolution following treatment of acoustic changes characteristic of turbulent respiratory gas flow due to wheezing and/or the incomplete resolution of atelectasis following the re-initiation of ventilation in a collapsed lung.


Description:

Anesthesiologists still rely on use of a conventional stethoscope to detect abnormal breath sounds during and after surgery - this process is labor intensive, intermittent, relies on human experience and thus is highly subjective. In fact, even for the most basic assessments, e.g. endobronchial intubation, human auscultation is unreliable.1 Digital stethoscopes are able to both amplify and digitize airway sounds and also provide a mechanism to record and analyze them for features undetectable by a human. Several small, pilot studies have shown that acoustic waveforms from the lungs produce characteristic spectral patterns in specific pulmonary pathophysiologic states. At this time, there are no studies that examine the acoustic patterns specific to perioperative wheezing or lung re-expansion. With the aid of computerized sound analysis, digital acoustic monitoring could provide a more sensitive, specific, and quantifiable indicator for perioperative respiratory abnormalities including wheezing. It is probable that the digital stethoscope has utility in the detection and monitoring of acoustic changes characteristic of turbulent respiratory gas flow due to wheezing and/or the incomplete resolution of atelectasis following the re-initiation of ventilation in a collapsed lung. In addition, treatment of perioperative wheezing with an inhaled bronchodilator may lead to resolution of wheezing and this response to treatment may also be monitored using waveform and spectral characteristics of the acoustic patterns from the digital stethoscope.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date August 27, 2021
Est. primary completion date August 27, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Patients scheduled for either: 1. open thoracic or video-assisted thoracoscopic surgery under general anesthesia requiring one-lung ventilation 2. abdominal surgery with a known history of chronic obstructive pulmonary disease (as documented in the electronic medical record) Exclusion Criteria: - Emergency surgery - surgery requiring the use of transesophageal echocardiography - refusal of informed consent - pregnancy - esophageal surgery - lung transplantation - contraindications for placement of esophageal stethoscope including esophageal varices strictures, motility disorders, diverticula or a history of prior esophageal injury or surgery - age less than 18 years old - prisoner

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Acoustic ventilation
Placement and removal of the esophageal stethoscope Connection of a microphone to the esophageal stethoscope outside of and removed from the patient's body at the location on the figure above "Connection fo monaural earpiece." Digital breath sound real-time monitoring will be collected as .wav files from the device with no identifiable elements and the data from the device will be downloaded onto a desktop and we will keep and store the data on a secure departmental server. Additional monitoring schedule includes evaluation of breath sounds with a conventional stethoscope every 30 minutes intraoperatively, at the start of one-lung ventilation, at the return to two-lung ventilation and prior to extubation and during any changes on the digital breath sounds recording monitor.

Locations

Country Name City State
United States University of Virginia Charlottesville Virginia

Sponsors (1)

Lead Sponsor Collaborator
University of Virginia

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Spectral Waveform Analysis to discriminate between wheezing and not wheezing based on specific frequency bands Comparison of the spectral waveforms to determine the specific frequency bands associated with wheezing and non-wheezing Duration of the operation while the esophageal stethoscope is in place, an average of 3 hours
Secondary Spectral waveform analysis associated with ventilatory parameters Ventilatory parameters including respiratory rate, tidal volume, and airway pressures that were recorded during the case will be compared with the spectral waveforms to determine the specific frequency bands associated with ventilatory parameters during one-lung ventilation and two-lung ventilation Duration of the operation while the esophageal stethoscope is in place, an average of 3 hours
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