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Trial registered on ANZCTR
Registration number
ACTRN12618000551291
Ethics application status
Approved
Date submitted
11/01/2018
Date registered
12/04/2018
Date last updated
4/09/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Does mouth gag application during Tonsillectomy or Adentonsillectomy alter optic nerve sheath diameter?
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Scientific title
Effect of Mouth Gag on Optic Nerve Sheath Diameter in Patients Undergoing Tonsillectomy or Adenotonsillectomy
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Secondary ID [1]
293541
0
nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
none
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Health condition
Health condition(s) or problem(s) studied:
tonsillectomy
305748
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adenotonsillectomy
305749
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Condition category
Condition code
Oral and Gastrointestinal
304962
304962
0
0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Surgery
304965
304965
0
0
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Other surgery
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
In this study we are using a rapid ultrasound procedure to the eye to look at the optic nerve sheath (ONS) diameter. The ultrasound will be applied by anesthesist who is certified to use ultrasound. The ultrasound scan involves gentle placement of an ultrasound probe on the closed eyelid of generally anesthetized patient undergoing tonsillectomy or adenotonsillectomy. The ultrasound will be applied as with the patient supine horizontally, a two-dimensional axial cross-sectional view of the ONSD will be obtained by positioning a 6-13 MHz transducer transversely on a single closed eyelid. On the ultrasound monitor, the ONSD will be measured 3 mm posterior to the orbital globe. Each measurement will be performed on the same orbit ONS diameter measurements will be compared at four time frames (after anesthesia induction, after tracheal intubation, after mouth gag application, 30 minutes after application)
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Intervention code [1]
299787
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Not applicable
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Comparator / control treatment
no control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
304146
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Change in optic nerve sheath diameter as assessed by rapid ultrasound scan after general anaesthesia induction, after tracheal intubation, mouth gag insertion and 30 minutes after mouth gag insertion
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Assessment method [1]
304146
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Timepoint [1]
304146
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After general anesthesia induction, after endotracheal intubation, after mouth gag insertion (primary timepoint), 20 minutes after mouth gag insertion
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Secondary outcome [1]
341099
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Change in mean arterial pressure by using blood pressure monitor on the anesthesia workstation
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Assessment method [1]
341099
0
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Timepoint [1]
341099
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After general anaesthesia induction, after endotracheal intubation, after mouth gag insertion, 30 minutes after mouth gag insertion and mouth gag while still in the mouth
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Secondary outcome [2]
343989
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Change in heart rate by using electrocardiogram on the anesthesia workstation
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Assessment method [2]
343989
0
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Timepoint [2]
343989
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After general anaesthesia induction, after endotracheal intubation, after mouth gag insertion, 30 minutes after mouth gag insertion
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Secondary outcome [3]
351473
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The relationship between the optic nerve sheath diameter and the angle between the Frankfurt plane and horizantal plane of the operation table in natural position as calculated by using an application (Angles in Photos, 2015 kublaidos) after mouth gag insertion
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Assessment method [3]
351473
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Timepoint [3]
351473
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After mouth gag insertion
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Eligibility
Key inclusion criteria
Patients aged between 3-18 and with an ASA physical status I-II and undergoing tonsillectomy or adenotonsillectomy will be included to the study.
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Minimum age
3
Years
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Maximum age
18
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
Exclusion criteria will be preexisting acute or chronic eye disease, history of eye surgery, use of drugs known to influence intraocular pressure (IOP) (ß blockers, Ca channel blockers, statins and nitrates) patients' parental refusal.
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Study design
Purpose
Natural history
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Duration
Cross-sectional
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Selection
Convenience sample
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Timing
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/05/2018
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Actual
1/05/2018
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Date of last participant enrolment
Anticipated
1/07/2018
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Actual
5/07/2018
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Date of last data collection
Anticipated
1/07/2018
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Actual
5/07/2018
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Sample size
Target
35
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Accrual to date
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Final
35
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Recruitment outside Australia
Country [1]
9480
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Turkey
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State/province [1]
9480
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Mugla
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Funding & Sponsors
Funding source category [1]
298155
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Hospital
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Name [1]
298155
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Mugla Sitki Kocman University Training and Research Hospital
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Address [1]
298155
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Kotekli Mahalllesi Mugla Sitki Kocman University Training and Research Hospital, Anesthesiology and Reanimation Department,48001, Mugla, Turkey
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Country [1]
298155
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Turkey
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Primary sponsor type
Individual
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Name
BASAK ALTIPARMAK
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Address
Kötekli Mahallesi Mugla Sitki Kocman University Training and Research Hospital, Anesthesiology and Reanimation Department, Mugla, 48001, Turkey
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Country
Turkey
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Secondary sponsor category [1]
297245
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None
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Name [1]
297245
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Address [1]
297245
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Country [1]
297245
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
299170
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MUGLA SITKI KOCMAN UNIVERSITY ETHICS COMMITTEE
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Ethics committee address [1]
299170
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Kötekli mahallesi, Mugla Sitki Kocman University Scientific Researches Ethics Committee Secretariat Mugla, 48001, Turkey
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Ethics committee country [1]
299170
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Turkey
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Date submitted for ethics approval [1]
299170
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02/10/2017
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Approval date [1]
299170
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02/03/2018
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Ethics approval number [1]
299170
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Summary
Brief summary
Our aim is to evaluate changes in the optic nerve sheath diameter (ONSD) in patients undergoing tonsillectomy adenoidectomy/tonsillectomy surgery while mouth gag is opened at the mouth.After obtaining approval from the Mugla Sitki Kocman Scientific Clinical Researches Ethics Committee 40 patients, 3 to 18 years old with an American Society of Anesthesiologists physical status of I and II scheduled for tonsillectomy, adenoidectomy, tonsiladenoidectomy will be enrolled into the study. Patients with the following conditions will be excluded: hypertension, preexisting acute or chronic eye disease, history of eye surgery, use of drugs known to influence IOP, expected duration of mouth gag opening <30 min. ONSD will be measured in all patients by an anesthesiologist trained in this procedure. With the patient supine horizontally, a two-dimensional axial cross-sectional view of the ONSD will be obtained by positioning a 12-MHz transducer transversely on a single closed eyelid. On the ultrasound monitor, the ONSD will be measured 3 mm posterior to the orbital globe. Each measurement will be performed on the same orbit. ONS diameter measurements will be compared at four time frames (after anesthesia induction, after tracheal intubation, after mouth gag application, 30 minutes after application. The baseline ONSD and the measurements at the time frames will be compared. In addition end tidal CO2 and mean arterial pressure will be assessed and recorded for every time point.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
79530
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A/Prof BASAK ALTIPARMAK
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Address
79530
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Kotekli Mahallesi Mugla Sitki Kocman University Training And Research Hospital Anesthesiology and Reanimation Department, Mugla, 48001, Turkey
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Country
79530
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Turkey
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Phone
79530
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+905326726533
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Fax
79530
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Email
79530
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[email protected]
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Contact person for public queries
Name
79531
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BASAK ALTIPARMAK
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Address
79531
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Kotekli Mahallesi Mugla Sitki Kocman University Training And Research Hospital Anesthesiology and Reanimation Department, Mugla, 48001, Turkey
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Country
79531
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Turkey
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Phone
79531
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+905326726533
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Fax
79531
0
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Email
79531
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[email protected]
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Contact person for scientific queries
Name
79532
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MELIKE KORKMAZ TOKER
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Address
79532
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Kotekli Mahallesi Mugla Sitki Kocman University Training And Research Hospital Anesthesiology and Reanimation Department, Mugla, 48001, Turkey
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Country
79532
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Turkey
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Phone
79532
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+905054747098
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Fax
79532
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+905054747099
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Email
79532
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[email protected]
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No information has been provided regarding IPD availability
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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