Actively Recruiting
Ultrasound-Guided Thyroid Cartilage Plane Block vs Ultrasound-Guided Traditional Superior Laryngeal Nerve Block for Awake Fiberoptic Intubation in Patients With Limited Neck Mobility Undergoing Cervical Spine Fixation
Led by Beni-Suef University · Updated on 2024-07-03
50
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of the work to compare between the effectiveness and safety of ultrasound-guided superior laryngeal nerve block through surface injection of local anesthetic solution on the thyroid cartilage and ultrasound-guided traditional superior laryngeal nerve block on quality of airway anesthesia for awake fiberoptic intubation in patients with limited neck mobility undergoing cervical spine fixation.
CONDITIONS
Official Title
Ultrasound-Guided Thyroid Cartilage Plane Block vs Ultrasound-Guided Traditional Superior Laryngeal Nerve Block for Awake Fiberoptic Intubation in Patients With Limited Neck Mobility Undergoing Cervical Spine Fixation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged between 18 and 65 years
- Any gender
- American Society of Anesthesiologists (ASA) physical status I or II
- Limited neck mobility
You will not qualify if you...
- Patients who refuse to give consent
- Non-cooperative patients
- Patients with asthma or ischemic heart disease
- Patients with preoperative hoarseness or sore throat
- Patients with mental or neurological disorders
- Contraindications for regional block such as coagulopathy, infection at the needle insertion site, or allergy to local anesthetics
- Body mass index (BMI) greater than 26 kg/m2
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beni-Suef University hospital
Banī Suwayf, Beni Suweif Governorate, Egypt, 62814
Actively Recruiting
Research Team
D
Dina M Fakhry, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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