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Trial registered on ANZCTR
Registration number
ACTRN12616001298404
Ethics application status
Approved
Date submitted
26/08/2016
Date registered
15/09/2016
Date last updated
13/12/2019
Date data sharing statement initially provided
16/01/2019
Date results provided
16/01/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Randomized Comparative Study of CMAC D blade versus Glidescope in Simulated Difficult intubations, Using manual inline cervical stabilization on patients with no difficult airway predictors
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Scientific title
Randomized Comparative Study of CMAC D blade versus Glidescope in Simulated Difficult intubations, Using manual inline cervical stabilization on patients with no difficult airway predictors
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Secondary ID [1]
290023
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NONE
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Universal Trial Number (UTN)
U1111-1183-4062
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Airway management
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Simulated difficult airway management using video laryngoscopes with manual in line axial stabilization on patients coming for elective surgery with no predictors of difficult airway
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Condition category
Condition code
Anaesthesiology
299941
299941
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0
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Anaesthetics
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The CMAC D blade and Glidescope are essentially meant for difficult intubations. In this present study we are comparing these two laryngoscopes in managing the difficult intubations. The limited extension of the neck will be simulated in patients with normal arirway anatomy, using manual in line axial stabilisation (MIAS) manouvre. CMAC D Blade is specially designed blade recommended by the manufacturer in managing the difficult airways. In this study we are testing the efficacy of CMAC D blade against Glidescope. MIAS is applied by an assistant ,standing beside the patient in front of the laryngoscopist with hands placed on the sides of the patient’s head and forearms resting on the patient’s chest. laryngoscopy will be done by single experienced anesthetist of consultant grade. Failure to intubate is defined as time taken to intubation exceeding more than 120 seconds or more than three unsuccessful attempts. The laryngoscopist grade the Intubation difficulty as per the Intubation Difficulty Scale Score (IDS). As per IDS score 0 score will be no difficulty and infinite score is impossible to intubate.
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Intervention code [1]
295740
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Treatment: Devices
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Comparator / control treatment
Comparator is Glidescope . Its essentially indirect videolaryngoscope and specially meant for difficult airway management. MIAS manouvre will be employed in this group also
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Control group
Active
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Outcomes
Primary outcome [1]
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Intubation difficulty scale score ( IDS)
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Assessment method [1]
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Timepoint [1]
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After successful tracheal intubation. The IDS score is graded by the laryngoscopist
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Primary outcome [2]
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Time taken for successful intubation. This is recorded using a stopwatch.
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Assessment method [2]
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Timepoint [2]
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The time counted from initial attempts to intubate from the end of bag and mask ventilation till the appearance end tidal carbon dioxide
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Secondary outcome [1]
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Hemodynamic parameters which includes Heart Rate, Systolic Blood Pressure, Diastolic blood pressure and Mean arterial pressure. These parameters are composite measurement. The recording will be done using a multi-parameter monitor which has non invasive blood pressure, ECG, Pulse-oximetry,
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Assessment method [1]
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Timepoint [1]
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Pre-induction
Pre-intubation
Post intubation
Post intubation 3 min
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Eligibility
Key inclusion criteria
Patients undergoing elective surgery that require general anesthesia with endotracheal intubation.
No predictors for difficult airway: as defined by
Mouth opening more than 4 cms,
Thyromental distance > 6 cms.
Malampati grade 1 and 2.
No documented evidence of difficult airway
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Minimum age
18
Years
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Maximum age
65
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Trauma patients
Emergency surgery
Any clinical predictors of difficult airway
Burns patients.
Bronchial asthma, COPD, bronchiectasis
Recent history of chest infection < 4 weeks
Thoracic cage anatomical deformity.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Central randomization by computer
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computerised sequence generation
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
Students t test
Fischer Exact test
ANOVA
Chisquare test
Power of the study 80%
Alpha error 5%
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
17/10/2016
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Actual
4/12/2016
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Date of last participant enrolment
Anticipated
16/10/2017
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Actual
23/09/2018
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Date of last data collection
Anticipated
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Actual
23/09/2018
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Sample size
Target
60
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Accrual to date
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Final
60
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Recruitment outside Australia
Country [1]
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Bahrain
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State/province [1]
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Bahrain
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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KING HAMAD UNIVERSITY HOSPITAL
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Address [1]
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PO Box 24343 , Road 2835 Area 228
Muharraq Bahrain
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Country [1]
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Bahrain
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Primary sponsor type
Individual
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Name
SHAHID ADEEL
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Address
Consultant
Anesthesia and Pain Medicine
King Hamad University Hospital
PO Box 24343 , Road 2835 Area 228
Muharraq Bahrain
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Country
Bahrain
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Secondary sponsor category [1]
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Individual
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Name [1]
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Mahesh Chandrashekaraiah
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Address [1]
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Registrar
Anesthesia and Pain Medicine
King Hamad University Hospital
PO Box 24343 , Road 2835 Area 228
Muharraq Bahrain
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Country [1]
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Bahrain
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Director of Research and Ethics
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Ethics committee address [1]
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King Hamad University Hospital PO Box 24343 Area 228 Road 2835 Bahrain
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Ethics committee country [1]
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Bahrain
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Date submitted for ethics approval [1]
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17/05/2016
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Approval date [1]
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24/08/2016
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Ethics approval number [1]
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KHUH/Research/No. 151/2016
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Summary
Brief summary
he CMAC D blades and Glidescope are essentially meant for difficult intubations. In this present study we are comparing these two laryngoscopes in managing the difficult intubations. In C-spine injury scenarios, the standard positioning and intubation technique for direct laryngoscopy cannot be employed in order to minimize the cervical spine injury.In our study we are simulating a restricted neck movement using the application of manual in line axial stabilization [MIAS] maneuver in patients who are not having difficult air way predictors and no C-spine injuries, requiring general anesthesia with endotracheal intubation for their contemplated surgical procedures.In this study we will try to simulate a scenario which we normally come across in trauma patients with C-spine involvement. .In this study we are comparing the efficacy of CMAC D blade against Glidescope
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Trial website
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Trial related presentations / publications
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Public notes
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Attachments [1]
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/AnzctrAttachments/371379-Acceptance Letter - Dr. Shahid Adeel - CMAC vs Glidescope.pdf
(Ethics approval)
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Attachments [2]
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/AnzctrAttachments/371379-Acceptance Letter - Dr Shahid Adeel - CMAC vs Glidescope - Title corrected.pdf
(Ethics approval)
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Contacts
Principal investigator
Name
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Dr SHAHID ADEEL
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Address
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Consultant Anesthesia and Pain Medicine
King Hamad University Hospital
Area 228 Road 2835 PO Box 24343
Muharraq Bahrain
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Country
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Bahrain
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Phone
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+97317444258
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Mahesh Madhugiri Chandrashekaraiah
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Address
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Registrar,Anesthesia and Pain Medicine
King Hamad University Hospital
Area 228 Road 2835 PO Box 24343
Muharraq Bahrain
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Country
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Bahrain
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Phone
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+97333520323
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Mahesh Madhugiri Chandrashekaraiah
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Address
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Registrar, Anesthesia and Pain Medicine
King Hamad University Hospital
Area 228 Road 2835 PO Box 24343
Muharraq Bahrain
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Country
68576
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Bahrain
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Phone
68576
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+97333520323
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Fax
68576
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
The consent is taken from the patient only to use the data for the study purpose and not to disclose in Public Domain. This Study participants data cannot be disclosed in public domain without the consent and ethics committee approval
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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