RecruitingNot ApplicableNCT06601036
Sevoflurane Sedation as an Alternative for Awake Fiberoptic Intubation in Difficult Airway Patients
Sponsor
Tanta University
Enrollment
70 participants
Start Date
Sep 17, 2024
Study Type
INTERVENTIONAL
Conditions
Summary
The aim of this study is to compare patient satisfaction and intubating conditions with fiber optic intubation under sevoflurane sedation versus airway blocks in difficult airway patients
Eligibility
Min Age: 18 YearsMax Age: 50 Years
Inclusion Criteria4
- Age from 18 to 50 years.
- Both sexes.
- American Society of Anesthesiology (ASA) physical status I-II.
- Patients with difficult airway (Mallampati grade 3 and 4 with mouth opening less than 5 cm).
Exclusion Criteria6
- Patient refusal.
- Patients with bleeding disorders and nasal mass.
- Allergy or intolerance to one of the study medications.
- Patients with uncontrolled systemic diseases.
- patients with gastro-esophageal reflex.
- history of nasopharyngeal surgery or drug abuse.
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Interventions
DRUGSevoflurane
Patients will undergo fiberoptic intubation under sevoflurane sedation.
DRUG2% Xylocaine (2 ml )
Patients will undergo fiberoptic intubation with bilateral Superior Laryngeal Nerve block and Recurrent laryngeal nerve block.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06601036
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