Actively Recruiting

Phase Not Applicable
Age: 21Years +
All Genders
NCT05455723

Tracheal Tube Cuff Inflation-Deflation Method for Video Assisted Laryngoscope Nasal Intubation in Adults

Led by Suez Canal University · Updated on 2025-01-31

90

Participants Needed

1

Research Sites

62 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare cuff inflation deflation method versus conventional method using Magill forceps in adult patients scheduled for elective surgery dental or maxillofacial that need nasal intubation. The study question: Is cuff inflation deflation method for nasal intubation takes a short time than the conventional method using Magill forceps in adult patients scheduled for elective surgery dental or maxillofacial? We will compare the inflation deflation technique with the Magill forceps technique for nasal intubation in adult patients to see if the inflation deflation technique will take less time and associated with less side effects like cuff perforation and mucosal injury. Participants will \[describe the main tasks participants will be asked to do, interventions they'll be given and use bullets if it is more than 2 items\].

CONDITIONS

Official Title

Tracheal Tube Cuff Inflation-Deflation Method for Video Assisted Laryngoscope Nasal Intubation in Adults

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • American Society of Anesthesiologists (ASA) physical status I-III
  • Scheduled for elective dental or maxillofacial surgery requiring nasal intubation
Not Eligible

You will not qualify if you...

  • Patients with coagulopathies
  • Patients with upper airway abnormalities
  • Patients at risk for aspiration
  • Patients who refuse to participate in the study

AI-Screening

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Trial Site Locations

Total: 1 location

1

Suez Canal University

Ismailia, Egypt, 41522

Actively Recruiting

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Research Team

T

Tarek F. Tammam, Professor

CONTACT

A

Aiman A. Al-Touny, Lecturer

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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