Clinical Trial

Asleep Fiberoptic vs Direct Laryngoscopy Effect on Hemodynamic Stability Using Opioid Free Anesthesia Induction

Completed
View on ClinicalTrials.gov →
Summary
The goal of this clinical trial is to compare blood pressure and heart rate between the fiberoptic and direct oral intubation using opioid free anesthesia induction. Secondary objectives include comparing the time needed for intubation and the incidence of postoperative sore throat, hoarseness, and upper airway trauma in adults aging between 18 to 55 years, scheduled for elective surgery under general anesthesia. The main question it aims to answer is: Does fiberoptic intubation cause less hemodynamic instability than direct oral intubation using opioid free anesthesia induction?
Protocol Amendment History 4 changes
critical Trial completed 2026-08-11
notable Enrollment reduced: 90 -> 68 participants 2026-08-11
notable Primary completion pushed: 2026-01-01 -> 2026-06-09 2026-08-11
minor Completion pushed: 2026-01-01 -> 2026-06-09 2026-08-11
Trial Details
NCT Number NCT06487988
Lead Sponsor American University of Beirut Medical Center
Conditions Analgesics, Opioid, Anesthesia, General, Heart Rate, Blood Pressure
Enrollment 68 participants
Start Date 2024-09-11
Primary Completion 2026-06-09 (estimated)
Study Completion 2026-06-09 (estimated)
Updated on ClinicalTrials.gov 2026-08-10