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Videolaryngoscopy Versus Direct Laryngoscopy for Endotracheal Intubation of Obese Patients: a Prospective Randomized Trial

NCT07004621 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 268

Last updated 2025-06-04

No results posted yet for this study

Summary

Patients were randomly assigned (1:1) to either a Macintosh laryngoscope group ("Macintosh group") or a videolaryngoscope group ("Video group").

Conditions

  • Intubating Laryngeal Airway

Interventions

OTHER

measurment of intubation time in seconds

determine whether modern technologies such as videolaryngoscopy shorten intubation time.

Sponsors & Collaborators

  • Jagiellonian University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-01
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07004621 on ClinicalTrials.gov