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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04494802
Other study ID # Gastric insufflation
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 10, 2020
Est. completion date August 10, 2021

Study information

Verified date July 2020
Source Seoul National University Hospital
Contact Jin-Tae Kim, PhD
Phone 82-2-2072-3664
Email jintae73@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cuff inflation up to the maximum cuff pressure when using LMA flexible can cause sore throat and discomfort after the surgery, and if the surgery is unexpectedly prolonged, there can be a side effect that can cause ischemic damage around the neck. If keeping cuff pressure low will not increase gastric insufflation and there is no change in other outcome variables, keeping it low may have a positive effect on anesthesia management and outcome in children.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 230
Est. completion date August 10, 2021
Est. primary completion date August 10, 2021
Accepts healthy volunteers No
Gender All
Age group 1 Year to 6 Years
Eligibility Inclusion Criteria:

- pediatric patients undergoing general anesthesia with LMA flexible

Exclusion Criteria:

- Unstable vital sign, significant arrhythmia or hypotension, Shock

- anticipated difficult intubation or the patient who have facial deformity

- high risk of aspiration

- recent upper respiratory tract infection history

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
lower pressure
During the operation, cuff pressure of LMA flexible is maintained to 30cmH2O
higher pressure
During the operation, cuff pressure of LMA flexible is maintained to 50cmH2O

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of gastric insufflation(antrum) Incidence of gastric insufflation which was recognized in gastric antrum with ultrasound During the surgery(up to 3 hours)
Secondary The size of gastric antrum and body The size of gastric antrum and body assessed immediately after insertion of LMA flexible and after finishing the surgery During the surgery(up to 3 hours)
Secondary Time for insertion of LMA flexible Time for insertion of LMA flexible During the anesthesia induction(up to 1 hour)
Secondary Success rate of insertion of LMA flexible Success rate of insertion of LMA flexible During the anesthesia induction(up to 1 hour)
Secondary The number of insertion attempt The number of insertion attempt During the anesthesia induction(up to 1 hour)
Secondary The number and the type of additional manipulation for successful ventilation The number and the type of additional manipulation for successful ventilation During the surgery(up to 3 hours)
Secondary Ease of insertion of LMA flexible Ease of insertion of LMA flexible(very easy, easy, moerate, difficult, very difficult) During the anesthesia induction(up to 1 hour)
Secondary Incidence of gastric insufflation(body) Incidence of gastric insufflation which was recognized in gastric body with ultrasound During the surgery(up to 3 hours)
Secondary Incidence of gastric insufflation recognized with the ausculation Incidence of gastric insufflation recognized with the ausculation after finishing surgery During the surgery(up to 3 hours)
Secondary peak pressure observed before, during, after surgery peak pressure observed before, during, after surgery During the surgery(up to 3 hours)
Secondary oropharyngeal leak pressure oropharyngeal leak pressure will be assessed by setting the APL valve of the circle system at 30 cmH2O with fresh gas flow of 3 L/min after the surgery During the surgery(up to 3 hours)
Secondary the complication rate the complication rate such as desaturation, blood staining of LMA flexible, hoarseness, dental/lip/tongue injury, aspiration During the surgery and after surgery (up to 6 hours)
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