NCT01997541

Brief Summary

There will be a difference of the insertion depth between the types of the endotracheal tube.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
76

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2013

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

Study Start

First participant enrolled

June 1, 2013

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

July 15, 2013

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2013

Completed
2 months until next milestone

First Posted

Study publicly available on registry

November 28, 2013

Completed
Last Updated

November 28, 2013

Status Verified

November 1, 2013

Enrollment Period

4 months

First QC Date

July 15, 2013

Last Update Submit

November 27, 2013

Conditions

Intubation

Outcome Measures

Primary Outcomes (1)

  • the distance between endotracheal tube tip and carina

    within 1 minute after intubation

Study Arms (2)

plain tube

reinforced tube

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

American Society of Anesthesiologists physical status I, II patients scheduled for elective surgery with general anesthesia

You may qualify if:

  • undergoing surgery under general anesthesia -

You may not qualify if:

  • upper airway or pulmonary problems
  • neck and/or chest distortion
  • patients at risk for pulmonary aspiration of gastric content -

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kyung Hee University Hospital at Gangdong

Seoul, 134-090, South Korea

Location

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate professor

Study Record Dates

First Submitted

July 15, 2013

First Posted

November 28, 2013

Study Start

June 1, 2013

Primary Completion

October 1, 2013

Study Completion

October 1, 2013

Last Updated

November 28, 2013

Record last verified: 2013-11

Locations

KR(1)