Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

SaCoVLM™ video laryngeal mask for airway management by military medics

Official title: Evaluation of SaCoVLM™ Video Laryngeal Mask Airway for Airway Management by Inexperienced Military Medics: A Two-Phase Feasibility Study

Run by Charles University, Czech Republic · NCT07249983 · Data updated 2026-11-12

This project will test whether the SaCoVLM™ video laryngeal mask helps military medics with limited intubation experience manage airways safely during simulation and in sedated elective surgery patients.

More Airway Management trials

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment50 (estimated)
SponsorCharles University, Czech Republic
Academic / other
Locations1 site (Prague, Prague)
StatusRecruiting
StartedMarch 1, 2026
Main results expectedDecember 2026
Study endsJanuary 2027
Registry record updatedApril 21, 2026
Trial IDNCT07249983 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adult patients (ASA I–II) scheduled for elective surgery who require airway management and are treated by participating military medics with limited intubation experience.

Probably not a fit

Patients with known airway abnormalities, pregnancy, allergy to anesthetics, emergency airway needs, or other high‑risk airway conditions are unlikely to be included or to benefit from this approach.

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

What this trial studies

This is a prospective, two-phase interventional project training military medics with limited airway experience to use the SaCoVLM™ video laryngeal mask and then observing their performance in clinical cases. Phase 1 uses manikin-based simulation to measure device placement, visualization quality, and intubation success and times under controlled conditions. Phase 2 enrolls adult patients undergoing elective surgery under general anesthesia to record first-attempt success rates, insertion and intubation times, glottic visualization scores, and complication rates. The overall aim is to see if the device can enable safe and effective airway management in resource-limited and prehospital military settings.

Why it matters

Potential benefit: If successful, the device could allow medics with limited intubation experience to secure airways faster and with fewer complications in prehospital and resource-limited military settings.

How similar studies have gone: Other video-equipped supraglottic airway devices have shown promising improvements in glottic visualization and intubation success, but using SaCoVLM™ specifically with minimally trained medics has limited prior data.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Elective surgery
* ASA I-II
* need for airway management

Exclusion Criteria:

* Pregnancy
* known airway abnormalities
* allergy to anesthetics

Where it's running

  • Military University Hospital Prague
    Prague, Prague, Czechia
    Recruiting

Study contacts

  • Principal investigator: Michal Sotak, M.D., Ph.D. — Military University Hospital, Prague
  • Study coordinator: Jan Palenik, M.D.
  • Email: jan.palenik@uvn.cz
  • Phone: +420973203254

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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.