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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02981537
Other study ID # JHBahk_blocker
Secondary ID
Status Completed
Phase N/A
First received December 1, 2016
Last updated July 12, 2017
Start date October 2016
Est. completion date January 2017

Study information

Verified date July 2017
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to find a novel method for placing endobronchial blockers without fiberoptic guidance to provide one-lung isolation during anesthesia for thoracic surgery.


Recruitment information / eligibility

Status Completed
Enrollment 94
Est. completion date January 2017
Est. primary completion date January 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients scheduled for lung resection

Exclusion Criteria:

- refuse to enroll

- patients with lesions involving mainstem bronchi

- patients with anomalies in tracheobronchial tree

Study Design


Related Conditions & MeSH terms


Intervention

Device:
two-staged endobronchial blocker insertion
positioning endobronchial blockers in two-staged method
single-staged endobronchial blocker insertion
positioning endobronchial blockers in traditional single-staged method

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary location of endobronchial blocker immediately after the insertion of blocker by fiberoptic bronchoscope
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