Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 hour
Participants undergo measurement of ventilation and intubation parameters during induction of anesthesia.
1 visit (in-person)
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
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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