Binaural Sound Effects for General Anesthesia (BS)
The Effect of Preoperative Binaural Sound on Propofol Dose Required for Induction of General Anesthesia: a Randomized, Placebo-controlled Trial
30 minutes before entering the operating room, the anxiety score is evaluated using a visual analogue scale (VAS) score, and stereo headphones, which can transmit binaural beat, are put on. According to a computer-generated assignment table, subjects are divided into an experimental group and a control group.
Binaural beat is applied to the experimental group for 20 minutes, and a silent state is applied to the control group for 20 minutes. After entering the operating room, electrocardiogram, pulse oxymetry, non-invasive blood pressure monitor, and sensor for depth of anesthsia are attached. Before induction of anesthesia, the anxiety score is evaluated on a VAS, again.
For anesthesia induction, propofol is administered at a rate of 10 mg every 15 seconds over 5 seconds. Assess the amount of propofol administered until the response to voice ("Open your eyes.") is absent, the subject's eyelash reflex disappears, and the PSI reaches below 50. Discontinue propofol injection when all three assessments (unresponsiveness to voice, loss of eyelash reflexes, Patient Sate Index (PSI) ≤ 50) become positive.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
30 minutes before entering the operating room, anxiety is evaluated on a VAS score (0-100mm, a ruler without scale) and stereo headphones, which can transmit binaural beat, are put on. A third party unrelated to the experiment sees the randomization table and applies binaural sound to the experimental group and silent state (silent sound file) to the control group for 20 minutes.
The sound generator is a smartphone device, which is hung on the transport bed. The volume is set to a level corresponding to 60dB.
After entering the operating room, start monitoring vital signs and depth of anesthesia (PSI) by attaching an electrocardiogram, pulse oxymetry, non-invasive blood pressure monitor, and sedline. Prepare by connecting a 3-way at the most proximal part of the intravenous cannula. After changing the volume to 0, take off the headphones, and evaluate the anxiety score using VAS.
Preoxygenation with oxygen 8L/min is sufficient, and in order to reduce venous pain caused by propofol injection, 1% lidocaine 50mg is pre-administrated. For anesthesia induction, 10mg propofol is administered every 15 seconds for 5 seconds. Assess the amount and time of propofol administered until the response to the voice ("Open your eyes.") is absent, the patient's eyelash reflex disappears, and the PSI reaches below 50. Propofol is administered until all three evaluations (no response to voice, loss of eyelash reflexes, PSI ≤ 50) are positive. After that, propofol is not administered. During anesthesia induction, the concentration of the inhaled anesthetic is adjusted so that Psi is between 25-50, and the anesthesia process is the same for both groups.
Continuously monitor blood pressure, pulse, and Psi, and record the MAC value of the inhaled anesthetic immediately after tracheal intubation, vital signs, and Psi.
The raw data of EEG is stored through the Sedline sensor and additionally analyzed and evaluated. The primary endpoint is the dose of propofol administered until the response to the voice ("Open your eyes.") is absent
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Jeong-Hwa Seo, MD.,PhD.
- Phone Number: +82-10-55020551
- Email: eongpa@empas.com
Study Locations
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Seoul, Korea, Republic of
- Recruiting
- Seoul National University Hospital
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Contact:
- Jeong-Hwa Seo, MD, Ph D
- Phone Number: 82-2-2072-0641
- Email: eongpa@empas.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adult patients aged 20-50 who require general anesthesia
- Patients who are able to provide written consent to participate in the clinical trial, to understand the procedure of this clinical trial, and to fill out the questionnaire appropriately
- Patients with ASA physical status classification 1-2
- Patients weighing from 50 kg to 80 kg
Exclusion Criteria:
- Patients with hearing loss or using hearing aids
- Patients who received narcotic analgesics or sedative drugs within 1 week
- Patients with alcohol or drug dependence
- Patients with drug hypersensitivity to propofol
- Patients with arrhythmia, cardiovascular disease, and decreased heart function
- Patients with liver failure
- Patients who are judged to be inappropriate for this clinical trial according to the opinions of investigators
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Placebo Comparator: Control
A silent state (a wave file made without sound) is applied for at least 20 minutes from 20 minutes before arrival to the operating room.
The sound generator is a smartphone device, set the volume (at a volume corresponding to 60 dB in the experimental group), and hang it on the transport bed.
Upon arrival in the operating room, before anesthesia, the volume is adjusted to 0.
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Apply a wave file which is created in silence.
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Experimental: Binaural beat
In the experimental group, the binaural sound, which was produced by the beat of 2Hz difference, is applied for 20 minutes from 20 minutes before arrival to the operating room.
The sound generator is a smartphone device, set the volume corresponding to 60 dB, and hang it on the transport bed.
Upon arrival in the operating room, before anesthesia, the volume is adjusted to 0.
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Different frequencies are transmitted in both ears, causing beats.
The low frequency sound generated by beats induces brainwaves entrainment.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Propofol dose
Time Frame: Until the response to the voice ("Open your eyes.") becomes absent (up to 5minutes)
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The amount of propofol administered until the response to the voice ("Open your eyes.")
becomes absent
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Until the response to the voice ("Open your eyes.") becomes absent (up to 5minutes)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Propofol dose
Time Frame: until eyelash reflex disappears (up to 5minutes)
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Propofol dose administered until eyelash reflex disappears
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until eyelash reflex disappears (up to 5minutes)
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Propofol dose
Time Frame: until PSI falls below 50 (up to 5minutes)
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Propofol dose administered until PSI falls below 50
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until PSI falls below 50 (up to 5minutes)
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Anxiety
Time Frame: 20minutes before the entrance to the operating room
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Anxiety is evaluated using VAS score(0-100mm ruler without a scale), 20minutes before the entrance to the operating room
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20minutes before the entrance to the operating room
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Anxiety
Time Frame: just before induction of anesthesia
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Anxiety is evaluated using VAS score(0-100mm ruler without a scale), just before induction of anesthesia
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just before induction of anesthesia
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Brainwaves
Time Frame: From the time you enter the operation room until the anesthesia induction is complete (up to 30minutes)
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brainwaves (raw data) which are collected in the Sedline device
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From the time you enter the operation room until the anesthesia induction is complete (up to 30minutes)
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Collaborators and Investigators
Investigators
- Principal Investigator: Jeong-Hwa Seo, MD.,PhD., Seoul National University Hospital
Publications and helpful links
General Publications
- Padmanabhan R, Hildreth AJ, Laws D. A prospective, randomised, controlled study examining binaural beat audio and pre-operative anxiety in patients undergoing general anaesthesia for day case surgery. Anaesthesia. 2005 Sep;60(9):874-7. doi: 10.1111/j.1365-2044.2005.04287.x.
- Facco E, Stellini E, Bacci C, Manani G, Pavan C, Cavallin F, Zanette G. Validation of visual analogue scale for anxiety (VAS-A) in preanesthesia evaluation. Minerva Anestesiol. 2013 Dec;79(12):1389-95. Epub 2013 Jul 9.
- Schmid W, Marhofer P, Opfermann P, Zadrazil M, Kimberger O, Triffterer L, Marhofer D, Klug W. Brainwave entrainment to minimise sedative drug doses in paediatric surgery: a randomised controlled trial. Br J Anaesth. 2020 Sep;125(3):330-335. doi: 10.1016/j.bja.2020.05.050. Epub 2020 Jul 8.
- Turkistani A, Abdullah KM, Al-Shaer AA, Mazen KF, Alkatheri K. Melatonin premedication and the induction dose of propofol. Eur J Anaesthesiol. 2007 May;24(5):399-402. doi: 10.1017/S0265021506001505. Epub 2006 Nov 10.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2204-007-1313
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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