Actively Recruiting
Comparison Between Nasal and Oropharyngeal Bleeding in Video Laryngoscopy and Direct Laryngoscopy for Nasal Intubation
Led by Aswan University · Updated on 2025-02-21
64
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of this study is to compare the effectiveness and safety of video laryngoscopy versus direct laryngoscopy for nasal intubation in patients with maxillofacial fractures regarding less bleeding to oral and nasal structures, quicker intubation times, increased success rates for first intubation attempts, fewer uses of the Magill forceps and the less need for cervical spine extension
CONDITIONS
Official Title
Comparison Between Nasal and Oropharyngeal Bleeding in Video Laryngoscopy and Direct Laryngoscopy for Nasal Intubation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients scheduled for maxillofacial surgeries requiring nasotracheal intubation
- ASA physical status I or II
- Body mass index (BMI) less than 35
You will not qualify if you...
- Bleeding disorders or abnormal blood clotting tests (PT, PTT, or platelet count)
- Local causes of bleeding such as adenoid issues
- Use of blood-thinning medications like anticoagulants or antiplatelets
- Failure of intubation in both nostrils or need for a tube smaller than 6.0 mm internal diameter
- Anticipated difficult airway
- ASA physical status III or IV
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Aswan University
Aswān, Aswan Governorate, Egypt, 81528
Actively Recruiting
Research Team
S
Soudy S Hammad, MD
CONTACT
M
Mohammed E Yahia, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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