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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05513989
Other study ID # IRB00006379 MMF
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2022
Est. completion date January 1, 2023

Study information

Verified date August 2022
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

compare between Magill forceps and modified pediatric Magill forceps for nasotracheal intubation (which method is easier and better?).


Description:

Group A One hundred and ten patients for whom modified pediatric Magill forceps was used to assist nasotracheal intubation. Group B One hundred and ten patients for whom Magill forceps was used to assist nasotracheal intubation. For each patient, intubation time, number of intubation attempts, hypoxia (recognized when oxygen saturation decreases below 94%), pharyngeal trauma, and need for corkscrewing will be recorded.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date January 1, 2023
Est. primary completion date January 1, 2023
Accepts healthy volunteers No
Gender All
Age group 4 Years to 8 Years
Eligibility Inclusion Criteria: - Patients with the American Society of Anesthesiology physical status of 1 or 2 - Age 4 to 8 years old. - Elective dental surgeries. Exclusion Criteria: - Parental refusal to consent (absolute contraindication), - Patients with aspiration risk. - Known upper airway abnormalities. - Those having difficult airway.

Study Design


Related Conditions & MeSH terms

  • Endotracheal Tube Wrongly Placed During Anesthetic Procedure

Intervention

Device:
modified Magill forceps
modified pediatric Magill forceps was used to assist nasotracheal intubation.
Magill forceps
Magill forceps was used to assist nasotracheal intubation.

Locations

Country Name City State
Egypt Ain shams university Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary intubation time just after anesthesia induction for 30 minutes
Secondary number of intubation attempts after anesthesia induction for 30 minutes
Secondary hypoxia after anesthesia induction for 30 minutes
Secondary pharyngeal trauma after intubation for 30 minutes
Secondary need for corkscrewing after anesthesia induction for 30 minutes
See also
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Completed NCT02691468 - Displacement Between PVC and Silicon DLT N/A
Completed NCT03031548 - Intra-op POCUS for Identification of Endotracheal Tube Position in the Pediatric Population