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

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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?

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 55
Healthy Volunteers: t
View:

• ASA (American Society of Anesthesiologists) physical status I and II

• Range age of 18-55 years' old

• Scheduled for elective surgery under general anesthesia.

Locations
Other Locations
Lebanon
Christian Rouphael
RECRUITING
Beirut
Contact Information
Primary
Christian Rouphael, MD
cr30@aub.edu.lb
01 350 000
Backup
Thuraya HajAli, MSc
th64@aub.edu.lb
01 350 000
Time Frame
Start Date: 2024-09-11
Estimated Completion Date: 2025-11-01
Participants
Target number of participants: 90
Treatments
Active_comparator: The direct conventional laryngoscopy group
The direct conventional laryngoscopy group will be performed with N3 (for females) or N4 (for males) Macintosh laryngoscope blade.
Experimental: The fiberoptic guided intubation group
The fiberoptic guided intubation will be performed.
Related Therapeutic Areas
Sponsors
Leads: American University of Beirut Medical Center

This content was sourced from clinicaltrials.gov