The VL3 Videolaryngoscope for Elective Tracheal Intubation in Adults

NCT ID: NCT04252222

Last Updated: 2020-02-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 56 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-12-04
• Study Completion Date: 2019-04-01

Brief Summary

We conducted an observational prospective pilot study to assess the efficacy of the VL3 videolaryngoscope for routinely tracheal intubation in 56 adults, in terms of successful rate, no. attempts and manoeuvre duration, including both normal and difficult airways.

Conditions

Difficult Airway Intubation

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

VL3

Tracheal intubation with VL3 videolaryngoscope

Group Type: EXPERIMENTAL

Videolaryngoscopy with VL3

Intervention Type: DEVICE

Tracheal Intubation aided by VL3 Videolaryngoscope

Interventions

Videolaryngoscopy with VL3

Tracheal Intubation aided by VL3 Videolaryngoscope

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Patients candidates for general anesthesia in elective surgery
• Age over 18 years
• ASA physical status I-III.

Exclusion Criteria

• Paediatric population
• ASA physical status IV
• Emergency tracheal intubation

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Campus Bio-Medico University

OTHER

Sponsor Role: lead

Responsible Party

Giuseppe Pascarella

Medical Doctor, Unit of Anesthesia and Intensive Care

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Università Campus Biomedico

Roma, , Italy

Countries

Italy

Other Identifiers

82/18 OSS ComET CBM

Identifier Type: -

Identifier Source: org_study_id