The Method to Reduce Displacement of Double-lumen Tube

December 7, 2011 updated by: Seoul National University Hospital

The Method to Reduce Displacement of Double-lumen Tube During Patient Positioning

The purpose of this study is to devise the method to reduce displacement of a left-sided double-lumen tube during patient positioning.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Anticipated)

100

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Seoul, Korea, Republic of, 110-744
        • Seoul National University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • patients undergoing thoracic surgery that require the placement of left-sided double-lumen tubes

Exclusion Criteria:

  • intraluminal lesion of left bronchus
  • very distorted anatomy of tracheobronchial tree

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: pillow
confirmation of double-lumen tube position with a head on a pillow
bronchoscopic confirmation of double-lumen tube position with a head on a pillow
Experimental: neutral
confirmation of double-lumen tube position in neutral position of a head
bronchoscopic confirmation of double-lumen tube position in neutral position of a head

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
tracheal displacement
Time Frame: up to 5 minutes
up to 5 minutes

Secondary Outcome Measures

Outcome Measure
Time Frame
bronchial displacement
Time Frame: up to 5 minutes
up to 5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2011

Primary Completion (Actual)

December 1, 2011

Study Completion (Actual)

December 1, 2011

Study Registration Dates

First Submitted

August 9, 2011

First Submitted That Met QC Criteria

August 9, 2011

First Posted (Estimate)

August 10, 2011

Study Record Updates

Last Update Posted (Estimate)

December 8, 2011

Last Update Submitted That Met QC Criteria

December 7, 2011

Last Verified

December 1, 2011

More Information

Terms related to this study

Other Study ID Numbers

  • JHBahk_DLT_pillow

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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