NCT03878797

Brief Summary

Virtual experiment : comparing the new method with conventional method of determining the depth of endotracheal intubation.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2019

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 15, 2019

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 18, 2019

Completed
2 months until next milestone

Study Start

First participant enrolled

May 20, 2019

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 26, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 26, 2019

Completed
Last Updated

January 18, 2020

Status Verified

January 1, 2020

Enrollment Period

7 months

First QC Date

March 15, 2019

Last Update Submit

January 14, 2020

Conditions

Endotracheal Intubation

Keywords

Endotracheal tubeEndobronchial intubationVocal cordsBronchoscopy

Outcome Measures

Primary Outcomes (1)

  • the depth of primary insertion of tracheal tube

    in a minute after intubation

Secondary Outcomes (3)

  • the distance from the corner of mouth to the carina

    in a minute after intubation

  • the distance from the vocal cords to the carina

    in a minute after intubation

  • the distance from the corner of mouth to the vocal cords

    in a minute after intubation

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

adult patients who are scheduled for elective surgery under general anesthesia

You may qualify if:

  • Patients who are scheduled for elective surgery under general anesthesia

You may not qualify if:

  • Patients with anatomical defects of the face, neck, or upper airway
  • Patients at risk for pulmonary aspiration of gastric content

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The First Affiliated Hospital with Nanjing Medical University

Nanjing, Jiangsu, 210029, China

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Director

Study Record Dates

First Submitted

March 15, 2019

First Posted

March 18, 2019

Study Start

May 20, 2019

Primary Completion

December 26, 2019

Study Completion

December 26, 2019

Last Updated

January 18, 2020

Record last verified: 2020-01

Locations

CN(1)