Clinical trial Recruiting at 1 site Observational Ages 18 and up

Predicting Difficult Awake Tracheal Intubation with Flexible Bronchoscopes

Official title: Classification and Prediction of Difficult Awake Tracheal Intubation With Flexible Bronchoscopes

Run by Universitätsklinikum Hamburg-Eppendorf · NCT06953414 · Data updated 2026-11-12

This study is testing a new way to predict if patients will have a hard time with awake tracheal intubation to help make the process safer for those with difficult airways.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment313 (estimated)
SponsorUniversitätsklinikum Hamburg-Eppendorf
Academic / other
Locations1 site (Hamburg, Free and Hanseatic City of Hamburg)
StatusRecruiting
StartedApril 30, 2025
Main results expectedJanuary 31, 2026
Study endsJanuary 31, 2026
Registry record updatedMay 6, 2025
Trial IDNCT06953414 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients aged 18 and older who have an anticipated difficult airway and are scheduled for awake tracheal intubation.

Probably not a fit

Patients who are not scheduled for awake tracheal intubation or those who are pregnant or breastfeeding may not benefit from this study.

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 develop and validate a classification system for predicting difficult awake tracheal intubation using flexible bronchoscopes. It addresses the lack of a tailored classification for this specific airway management technique, which is crucial for reducing anesthesia-related complications. The study will involve patients with anticipated difficult airways who are scheduled for awake intubation, and it will utilize multivariable prediction models to enhance the diagnostic accuracy of airway operators. By comparing existing classification tools with the new model, the study seeks to improve patient safety during anesthesia.

Why it matters

Potential benefit: If successful, this study could significantly enhance the safety and effectiveness of airway management in patients requiring difficult intubation.

How similar studies have gone: While there is a lack of specifically tailored classifications for this technique, existing studies on airway management have shown varying degrees of success, indicating that this approach may provide valuable insights.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients with an anticipated difficult airways scheduled for ATI:FB
* Consent by the patient
* Minimum 18 years of age

Exclusion Criteria:

* Patients not scheduled for ATI:FB
* Pregnant or breastfeeding patients
* Consent not given by the patient

Where it's running

  • University Medical Center Hamburg-Eppendorf
    Hamburg, Free and Hanseatic City of Hamburg, Germany
    Recruiting

Study contacts

  • Principal investigator: Martin Petzoldt, MD, FEAMS — University Medical Center Hamburg-Eppendorf: Universitatsklinikum Hamburg-Eppendorf
  • Study coordinator: Martin Petzoldt, MD, FEAMS
  • Email: m.petzoldt@uke.de
  • Phone: 04915222815932

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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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.