Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
150 participants
INTERVENTIONAL
2015-08-31
2016-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Didgital group
After induction of anesthesia, and after ensuring muscle relaxation, NGT will be inserted through the selected nostril and advanced for 12 cm then the NGT was advanced according to study group advancing. In control group; NGT was inserted with patient head flexed. In D group, after feeling the NGT in pharynx, with the head in neutral position,the index finger was used to support the NGT with slight direction towards the left side. This will prevent tube kinking at this point in front of the resistance offered by the inflated tube cuff or arytenoids cartilage. Also, this digital support reinforces the tube at the area weakened by its openings
Digital facilitation
Control group
No interventions assigned to this group
Interventions
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Digital facilitation
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
20 Years
60 Years
ALL
No
Sponsors
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Mansoura University
OTHER
Responsible Party
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AlRefaey Kandeel
DR
Locations
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Mansoura university
Al Mansurah, Dkahleya, Egypt
Countries
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Other Identifiers
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RefaNGT
Identifier Type: -
Identifier Source: org_study_id
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