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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03008473
Other study ID # 20161229
Secondary ID
Status Completed
Phase N/A
First received December 29, 2016
Last updated February 22, 2018
Start date January 2017
Est. completion date September 24, 2017

Study information

Verified date December 2016
Source The First Hospital of Qinhuangdao
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

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


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date September 24, 2017
Est. primary completion date September 24, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

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

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

Study Design


Related Conditions & MeSH terms

  • Therapeutic Procedural Complication

Intervention

Device:
video laryngoscope and chest CT iminge

Conventional intubation of uniblocker


Locations

Country Name City State
China The first hospital of Qinhuangdao Qinhuangdao Hebei

Sponsors (1)

Lead Sponsor Collaborator
The First Hospital of Qinhuangdao

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intubation Time 5min
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