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CompletedNCT03008473Updated Feb 23, 2018

Chest CT for the Placement of the Uniblocker

An interventional study of video laryngoscope and chest CT iminge and Conventional intubation of uniblocker in Therapeutic Procedural Complication, sponsored by The First Hospital of Qinhuangdao. Completed at 1 site in China. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2018-02-23.

Sponsored by The First Hospital of Qinhuangdao · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Video laryngoscope and chest CT iminge for the placement of the Uniblocker

Read the detailed description

Comparing the traditional method of Uniblocker intubation and video laryngoscope combined with chest CT iminge guide the precise localization of Uniblocker

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Conditions studied

  • Therapeutic Procedural Complication
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In context

Lead sponsor

The First Hospital of Qinhuangdao is the lead sponsor of 22 studies on the registry; 1 is open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

BMI less than 35 kg/m2 ASA classifications of I-III, Modified Mallampati classification 1 or 2 Under general anesthesia

Exclusion criteria

Exclusion Criteria:

  • Age younger than 18 yr or older than 65 yr
  • ASA class IV or V
  • Abnormalities of the heart, brain, liver, lung, kidney and coagulation functions
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
70 participants (actual)

Study arms

  • Experimental
    video laryngoscope and chest CT iminge

    First,the operator calculate the distance between the carina and the glottis by CT image and make a marker on the Uniblocker. Then the operator inserted the Uniblocker into the trachea and advanced toward the left main-stem bronchus via the video laryngoscope untill see marker just at the glottis then stopped the insertion .Second, a single lumen tube with appropriate size was intubated via video laryngoscope into the appropriate depth.Third,the Fiberoptic bronchoscopy(FOB) was inserted into single lumen tube to assess the position of the Uniblocker and the injuries of bronchi and carina

    Device: video laryngoscope and chest CT iminge

  • Experimental
    Conventional intubation of Uniblocker

    First, a conventional single lumen tube (SLT) was inserted into trachea at optimal depth via video laryngoscope. Second, a Uniblocker was inserted through SLT and directed to the left main-stem bronchus. Third, an FOB was inserted into the SLT to adjust the Uniblocker to optimal position and assessed the injuries of bronchi and carina.

    Device: Conventional intubation of uniblocker

Interventions

  • Devicevideo laryngoscope and chest CT iminge
  • DeviceConventional intubation of uniblocker
06

What researchers measure

Primary outcomes

  1. Intubation Time

    Time frame: 5min

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Study locations

1 site
  • The first hospital of Qinhuangdao
    Qinhuangdao, Hebei 066000, China
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References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 23, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03008473
Lead sponsor
The First Hospital of Qinhuangdao
Responsible party
Sponsor
First posted
Jan 2, 2017
Start date
Jan 2017
Primary completion
Sep 24, 2017
Completion
Sep 24, 2017
Last update
Feb 23, 2018

Study contacts

Ximing Qi, PHD
study director · The First Hospital of Qinhuangdao

Oversight

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

Not currently enrolling

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

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