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

> **NCT06487988** · NA · RECRUITING · sponsor: **American University of Beirut Medical Center** · enrollment: 90 (estimated)

## Conditions studied

- Analgesics, Opioid
- Anesthesia, General
- Heart Rate
- Blood Pressure

## Interventions

- **DEVICE:** direct conventional laryngoscopy
- **DEVICE:** fiberoptic guided intubation

## Key facts

- **NCT ID:** NCT06487988
- **Lead sponsor:** American University of Beirut Medical Center
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2024-09-11
- **Primary completion:** 2026-01-01
- **Final completion:** 2026-01-01
- **Target enrollment:** 90 (ESTIMATED)
- **Last updated:** 2025-12-19


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06487988

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06487988, "Asleep Fiberoptic vs Direct Laryngoscopy Effect on Hemodynamic Stability Using Opioid Free Anesthesia Induction". Retrieved via AI Analytics 2026-07-09 from https://api.ai-analytics.org/clinical/NCT06487988. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*