Actively Recruiting

Age: 18Years +
All Genders
ID07114549

External Validation of the MASCAN Score for the Classification of Difficult Mask Ventilation

Led by Universitätsklinikum Hamburg-Eppendorf · Updated on 2025-08-21

926

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the MASCAN Score, an objective tool developed to classify difficult facemask ventilation. This observational study aims to validate the MASCAN score in patients undergoing general anesthesia for surgical procedures. It also examines how different techniques, such as the timing of neuromuscular blocking agents and manual versus controlled facemask ventilation, influence outcomes. Secondary goals include assessing the diagnostic value of visual capnography curve evaluations and comparing the first attempt success rates during tracheal intubation as reported by the airway operator and an independent observer. Participants will undergo measurement of primary and secondary outcome parameters during the induction of anesthesia. The study focuses on patients receiving general anesthesia with facemask ventilation before tracheal intubation. Various ventilation parameters, airway events, and intubation details are recorded within one hour of induction to gather comprehensive data. During the study, participants will be monitored for factors such as difficult facemask ventilation, capnograph quality, ventilation mode changes, oxygen saturation levels, and airway-related adverse events. Researchers will evaluate intubation attempts, success rates, glottic view, and post-intubation recommendations. The study involves informed consent and includes patients aged 18 years or older scheduled for surgery requiring facemask ventilation and tracheal intubation. Participation involves close observation and data collection during anesthesia induction and airway management.

CONDITIONS

Brief Title

External Validation of the MASCAN Score for the Classification of Difficult Mask Ventilation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who are scheduled for surgery with general anesthesia and require facemask ventilation and tracheal intubation after induction of anesthesia
  • Patients aged 18 years or older
  • Provided informed consent
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding woman
  • Required rapid sequence induction or other contraindications for facemask ventilation
  • Planned awake tracheal intubation
  • No consent given

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 hour

Participants undergo measurement of ventilation and intubation parameters during induction of anesthesia.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 1 hour after induction

Participants are observed for airway-related outcomes and any post-intubation recommendations.

Observation during the same visit

Trial Site Locations

Total: 1 location

1

University Medical Center Hamburg-Eppendorf

Hamburg, Free and Hanseatic City of Hamburg, Germany, 20251

Actively Recruiting

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Research Team

M

Martin Petzoldt, MD

V

Viktor A Wünsch, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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