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Examination of Double-Lumen Tube Placement by Functional Electrical Impedance Tomography

This study has been completed.

Sponsored by: University Hospital Freiburg
Information provided by: University Hospital Freiburg
ClinicalTrials.gov Identifier: NCT00486616
  Purpose

The purpose of this study is to determine whether functional electrical impedance tomography is suitable for examination of double-lumen tube placement compared with fibreoptic evaluation.


Condition Intervention
Double-Lumen Tube Placement
One-Lung Ventilation
Device: electrical impedance tomography
Procedure: double-lumen tube placement

MedlinePlus related topics:   CT Scans   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Prospective
Official Title:   Examination of Double-Lumen Tube Placement: Functional Electrical Impedance Tomography Versus Fibreoptic Bronchoscopy

Further study details as provided by University Hospital Freiburg:

Study Start Date:   May 2007
Study Completion Date:   August 2007
Primary Completion Date:   August 2007 (Final data collection date for primary outcome measure)

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • consent of the patient
  • intubation with left- or right-sided double-lumen tube
  • age >= 18 years

Exclusion Criteria:

  • refusal by the patient
  • contraindications for EIT-measurement (e.g. pacemaker, pregnancy)
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00486616

Locations
Germany
University Hospital Freiburg    
      Freiburg, Germany, 79106

Sponsors and Collaborators
University Hospital Freiburg

Investigators
Principal Investigator:     Daniel Steinmann, MD     Department of Anesthesia and Critical Care Medicine, University Hospital Freiburg    
  More Information

Study ID Numbers:   117/07
First Received:   June 13, 2007
Last Updated:   February 11, 2008
ClinicalTrials.gov Identifier:   NCT00486616
Health Authority:   Germany: Federal Institute for Drugs and Medical Devices

ClinicalTrials.gov processed this record on September 04, 2008




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