Sevoflurane Sedation as an Alternative for Awake Fiberoptic Intubation in Difficult Airway Patients

NCT06601036 · tracked via the Priya Life Science Egypt tracker

Sponsor

Tanta University

Phase

Not applicable

Started

2024-09-17

Last updated

2024-09-19

Condition(s) studied

SevofluraneSedationAwake Fiberoptic IntubationDifficult Airway

Investigational drug(s) / intervention(s)

Sevoflurane →2% Xylocaine (2 ml ) →

Sevoflurane: Patients will undergo fiberoptic intubation under sevoflurane sedation.

2% Xylocaine (2 ml ): Patients will undergo fiberoptic intubation with bilateral Superior Laryngeal Nerve block and Recurrent laryngeal nerve block.

Study 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

Sex

ALL

Min age

18 Years

Max age

50 Years

Healthy volunteers

Inclusion Criteria: * 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 Criteria: * 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.

Primary outcome measure(s)

Degree of patient satisfaction — Immediately after intubation
The degree of patient satisfaction will be assessed on a 4-point Likert scale patient satisfaction (1, very dissatisfied; 2, unsatisfied; 3, satisfied; 4, very satisfied).

Trial sites (1)

Facility	City	Region	Status
Tanta University	Tanta	El-Gharbia	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06601036 on ClinicalTrials.gov ↗ ← All trials in Egypt