Overview
Ketamine Versus Lidocaine Nebulization for Awake Fiberoptic Intubation
Status:
Completed
Completed
Trial end date:
2019-07-25
2019-07-25
Target enrollment:
0
0
Participant gender:
All
All
Summary
This randomized double-blinded study is performed to compare ketamine versus lidocaine for nebulization for awake nasal fiberoptic intubation as regard efficacy and side effects.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Ain Shams UniversityTreatments:
Ketamine
Lidocaine
Criteria
Inclusion Criteria:- American Society of Anesthesiologists (ASA) physical status I and II of both sexes
with body weight from 60-90 kg, and planned for elective awake nasal fiberoptic
intubation due to expected difficulty in airway management (e.g. limited mouth
opening, trismus, mandibular/ maxillary swellings or tumors, ludwig's angina, or other
indications).
Exclusion Criteria:
- body weight < 60 kg or > 90 kg
- uncooperative, with mental or psychological problems
- known allergy to any of the study drugs
- pregnancy
- hypertension
- cardiac disease
- liver or renal impairment
- epilepsy,
- asthmatic,
- previous bad experience of awake intubation,
- emergency operations or
- coagulation abnormalities