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A Clinical Comparison of Three Bronchial Blockers for One-Lung Ventilation in Thoracic Surgery

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified September 2006 by University Health Network, Toronto.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00188916
First Posted: September 16, 2005
Last Update Posted: June 12, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University Health Network, Toronto
  Purpose
This is a clinical trial comparing surgical conditions during one-lung ventilation with three different bronchial blockers or with double-lumen endobronchial tubes.

Condition Phase
Thoracic Surgery Phase 4

Study Type: Observational
Study Design: Allocation: Random Sample
Time Perspective: Longitudinal
Time Perspective: Prospective

Further study details as provided by University Health Network, Toronto:

Estimated Enrollment: 120
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   16 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Criteria

Inclusion Criteria:

  • Left thoracotomy

Exclusion Criteria:

  • Contraindication to lung isolation
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00188916


Contacts
Contact: Peter Slinger, MD 416-340-5164 peter.slinger@uhn.on.ca

Locations
Canada, Ontario
University Health Network Recruiting
Toronto, Ontario, Canada, M5G 2C4
Contact: Peter Slinger, MD    416-340-5164      
Sponsors and Collaborators
University Health Network, Toronto
Investigators
Principal Investigator: Peter Slinger, MD University Health Network, Toronto
  More Information

ClinicalTrials.gov Identifier: NCT00188916     History of Changes
Other Study ID Numbers: UHN REB 04-0407-AE
First Submitted: September 13, 2005
First Posted: September 16, 2005
Last Update Posted: June 12, 2007
Last Verified: September 2006

Keywords provided by University Health Network, Toronto:
Bronchial blockers
Lung isolation
Thoracic Anesthesia