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NCT05721690: UED-VLG

UED-A Videolaryngoscope vs. Glidescope Titanium for Elective Tracheal Intubation

Completed NA Last updated 30 August 2023
What this trial tests

NA trial testing UED-A Videolaryngoscopy in Intubation; Difficult or Failed in 60 participants. Completed in 13 May 2023.

Timeline
1 February 2023
Primary endpoint
12 May 2023
13 May 2023

Quick facts

Lead sponsorCampus Bio-Medico University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment60
Start date1 February 2023
Primary completion12 May 2023
Estimated completion13 May 2023
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Campus Bio-Medico University

Who can join

18 and older, any sex, with Intubation; Difficult or Failed. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The present randomized clinical trial wants to compare the efficacy and safety of UED-A videolaryngoscope to Glidescope Titanium for routinely tracheal intubation in 60 adults, in terms of successful rate, no. attempts and manoeuvre duration.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Hyper-angulated (Glidescope) versus intermediate-angled (UED-A) videolaryngoscopy for routine tracheal intubation in adults: a prospective randomized controlled trial.
    Migliorelli S, Strumia A, Costa F, Puricelli G, et al · · 2026 · PMID 41535320 · DOI 10.1038/s41598-025-30932-3

Verify or expand the search:

Other recruiting trials for Intubation; Difficult or Failed

Currently open trials in the same condition.

Other Campus Bio-Medico University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05721690.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing