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The Depth of Right Bronchial Blocker Placement in Taiwanese in Video-assisted Thoracoscopic Surgery(VATS)

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01388803
Collaborator
(none)
60
Enrollment
1
Location
11
Duration (Months)
5.5
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

A retrospective study to demonstrate the optimal depth of right side bronchial blocker for complete right lung separation. Data were collected from all patients who completed right side VATS with right side BB from Jan 2010 through Nov 2010.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    After general anesthesia, an 8.0 mm internal-diameter single-lumen endotracheal tube was inserted orally. An independent Coopdech bronchial blocker, which has a formed-curvature near the catheter tip, was directly inserted through the single-lumen endotracheal tube into right main bronchus. Chest inspection, auscultation, fiberoptic bronchoscopy confirmation, if necessary, by visualizing the blocker cuff located at right main bronchus just below the carina was performed firstly. After placing patients in left decubitus position, the position of BB was reconfirmed by auscultation firstly; then complete collapse of the right upper lobe was adjust, if necessary and reconfirmed on the video of thoracoscopy by both surgeon and anesthesiologists. The depth of BB and the need of fiberoptic bronchoscope were recorded. All the patients were extubated in operation room after completion of operation with optimal analgesia. Data collected included; age, sex, body height and weight and the depth of right-sided BB from incisor was then recorded.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    60 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Retrospective
    Official Title:
    Right Side Bronchial Blocker in Video-assisted Thoracoscopic Surgery
    Study Start Date :
    Jan 1, 2010
    Actual Primary Completion Date :
    Nov 1, 2010
    Actual Study Completion Date :
    Dec 1, 2010

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years to 77 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:
      • Patients receiving right side VATS( video-assisted thoracoscopic surgery) with right side bronchial blocker
      Exclusion Criteria:
      • Patients receiving thoracic surgery with double lumen tubes

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 National Taiwan University Hospital Taipei Taiwan 100

      Sponsors and Collaborators

      • National Taiwan University Hospital

      Investigators

      • Study Director: ya-jung cheng, PhD, deaprtment of anesthesiology, national taiwan university hospital

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT01388803
      Other Study ID Numbers:
      • 201012143RC
      First Posted:
      Jul 7, 2011
      Last Update Posted:
      Jul 20, 2011
      Last Verified:
      Jul 1, 2011
      Keywords provided by , ,
      bronchial blocker
      VATS
      Additional relevant MeSH terms:
      Pneumothorax

      Study Results

      No Results Posted as of Jul 20, 2011