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NCT Number: NCT07681453

Blind Intubation Through the Tulip Airway Versus Direct Laryngoscopy

This is a randomized crossover mannequin study comparing two airway management techniques in novice operators: blind endotracheal intubation via the Tulip oropharyngeal airway versus direct laryngoscopy. The study aims to evaluate and compare the success rate and performance characteristics of both methods under simulated conditions in order to assess their effectiveness in airway management training and practice.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ankara Etlik City Hospital, Ministry of Health, Türkiye

Ankara, 06170, Turkey (Türkiye)

Location status: Recruiting

Location contact

Fethi Gültop, MD

CONTACT

[email protected]

+905052260067

About this study

This study is a randomized crossover mannequin-based simulation designed to compare two endotracheal intubation techniques performed by novice operators with limited or no prior intubation experience.

Participants will perform tracheal intubation using two different methods in a randomized order: (1) blind endotracheal intubation via the Tulip oropharyngeal airway, and (2) direct laryngoscopy. Each participant will serve as their own control in a crossover design, allowing direct comparison of the two techniques under standardized simulated airway conditions.

The primary objective is to compare the success rate of intubation between the two techniques. Secondary outcomes may include time to successful intubation, number of attempts, and ease of use, as assessed in a controlled simulation environment.

All procedures will be performed on airway mannequins in a simulation setting without involving human subjects or patient care. The study is intended to evaluate technical performance and feasibility in a standardized training environment, rather than clinical effectiveness in patients.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Voluntary participation in the study
  • Anesthesia technician students with no prior airway management experience
  • Age ≥ 18 years
  • Willingness to participate in simulation-based intubation procedures

Exclusion criteria

  • Prior advanced airway management experience (e.g., regular intubation practice in clinical settings)
  • Refusal to participate or withdraw consent
  • Inability to complete simulation procedures for any reason

Treatment and study plan

Tulip oropharyngeal airway

Device

Endotracheal intubation via Tulip airway in a simulated mannequin setting.

Direct Laryngoscopy

Procedure

Standard endotracheal intubation using direct laryngoscopy.

Primary outcomes

  1. First-pass intubation success rate

    Time frame: At each endotracheal intubation attempt during the single-day randomized crossover simulation session in a mannequin model

    Comparison of first-attempt success rate of endotracheal intubation using Tulip oropharyngeal airway versus direct laryngoscopy in a simulated mannequin setting performed by novice operators in a randomized crossover design.

Study contacts

Contact information is provided by the study sponsor or research team.

Fethi Gültop, MD

CONTACT

[email protected]

+90 505 2260067

Sponsors and collaborators

Lead sponsor

Ankara Etlik City Hospital

Other Gov

Registry information

Official study title

Comparison of Blind Endotracheal Intubation Through the Tulip Oropharyngeal Airway and Direct Laryngoscopy by Novice Operators: A Randomized Crossover Manikin Study

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 2, 2026
Registry last updated
Jul 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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