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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT02257411 |
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Date of registration:
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22/09/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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A Method to Determine the Size of Laryngeal Mask Airway (LMA)
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Scientific title:
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A Simple Method to Determine the Size of the ProSeal LMA (PLMA) in Children |
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Date of first enrolment:
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June 2013 |
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Target sample size:
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197 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT02257411 |
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Study type:
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Interventional |
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Study design:
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator)
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Phase:
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N/A
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Countries of recruitment
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Turkey
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- ASA physical status I/II
- scheduled for genitourinary operation
- LMA was indicated for anesthesia
Exclusion Criteria:
- surgery lasting more than 3 h
- overweight or underweight patients
- gastroesophageal reflux
- risk of aspiration
- airway infection in the last six weeks
- decreased pulmonary or chest wall compliance.
Age minimum:
N/A
Age maximum:
15 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Ear Based ProSeal LMA
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Intervention(s)
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Device: Ear-sized based
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Primary Outcome(s)
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the sizes of the PLMA determined with the ear-based formula
[Time Frame: One year]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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