Comparing sedation methods for awake fiberoptic intubation

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to evaluate the effectiveness of two sedation regimens during awake fiberoptic intubation in patients with potentially difficult airways. Participants will be randomized into two groups: one receiving a combination of midazolam, fentanyl, and a placebo, and the other receiving midazolam, fentanyl, and dexmedetomidine. The study will assess the impact of these sedation protocols on intubation conditions, patient satisfaction, and hemodynamic stability. Data will be collected from patient medical records and through a brief survey conducted 24 hours post-procedure.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Subjects with potentially difficult airways who require awake fiberoptic intubations will be identified from the OR schedule and the pre-operative clinic workups.

Exclusion Criteria:

* Anyone who does not meet the inclusion criteria

Where it's running

• University of Illinois
  Chicago, Illinois, United States Recruiting

Study contacts

• Principal investigator: David Glick, MD — Department of Anesthesiology Head
• Study coordinator: Alexandra Barabanova, MS
• Email: barabano@uic.edu
• Phone: (312)355-5733

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.