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The purpose of this current study is to compare changes of the intracuff pressure in the newly designed LMA with the older design LMA after insertion of an esophagogastroduodenoscopy (EGD) probe in pediatric patients and adolescents.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| New LMA or Old LMA | newly designed LMA or older designed LMA |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ambu LMA | Device | Will be randomized to either the new Gastro LMA or old Ambu LMA for EGD procedure and the intracuff pressure will be measured |
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| Measure | Description | Time Frame |
|---|---|---|
| Excessive intracuff pressure | Our primary goal is to compare the incidence of excessive intracuff pressure after EGD probe insertion between the newly designed LMA and the older version LMA. For this primary outcome, we will define excessive intracuff pressure as ≥40 cmH2O. | as long as the LMA is in place in the OR with usually a max amount of time of 45 minutes |
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Inclusion Criteria:
Exclusion Criteria:
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Patients who weigh more than 30 kg who are undergoing an EGD and who are getting an LMA at Nationwide Children's Hospital.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Nationwide Children's Hospital | Columbus | Ohio | 43205 | United States |
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| Gastro LMA | Device | Will be randomized to either the new Gastro LMA or old Ambu LMA for EGD procedure and the intracuff pressure will be measured |
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