ClinicalTrials.gg
Status unknownNCT02949856Updated Oct 31, 2016

E-T Tube Cuff Pressure Change After Changing Position From Neutral to Hyperextension of Neck

An interventional study of Mallinckrodt, COVIDIEN and Endotracheal tube, Unomedica in Thyroidectomy, sponsored by Keimyung University Dongsan Medical Center. Status unknown. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2016-10-31.

Sponsored by Keimyung University Dongsan Medical Center · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Oct 2016), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

This study evaluates difference of the endotracheal tube cuff pressure between a tapered- versus a cylindrical- shaped cuff after changing from neutral to hyperextension of neck.

Fifty patients undergoing thyroidectomy are randomly allocated into two groups (tapered- and cylindrical-shaped cuff). Endotracheal tube cuff pressure is initially set at 20 cmH20 in the supine neutral position and is measured after the change to the neck extension.

02

Conditions studied

  • Thyroidectomy
03

In context

Lead sponsor

Keimyung University Dongsan Medical Center is the lead sponsor of 86 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • American Society of Anesthesiologists physical classification 1-3, 18-70 year old, thyroidectomy

Exclusion criteria

Exclusion Criteria:

  • difficult intubation, history of cervical disease, motion limitation of neck, morbid obesity
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Single (Participant)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    Tapered

    Mallinckrodt, COVIDIEN

    Device: Mallinckrodt, COVIDIEN

  • Active comparator
    Cylindrical

    Endotracheal tube, Unomedical

    Device: Endotracheal tube, Unomedica

Interventions

  • DeviceMallinckrodt, COVIDIEN
  • DeviceEndotracheal tube, Unomedica
06

What researchers measure

Primary outcomes

  1. Change in intracuff pressure

    Time frame: 1 year

Secondary outcomes

  1. Change in distance from carina to tip of tube

    Time frame: 1 year

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 31, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02949856
Lead sponsor
Keimyung University Dongsan Medical Center
Responsible party
Sponsor
First posted
Oct 31, 2016
Start date
Oct 2016
Primary completion
Apr 2017 (estimated)
Completion
Jul 2017 (estimated)
Last update
Oct 31, 2016

Study contacts

Yong-Cheol Lee, MD, PhD
Contact
yclee@dsmc.or.kr
82-53-250-7193
Yong-Cheol Lee, MD, PhD
principal investigator · Keimyung University Dongsan Medical Center

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

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