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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00188916
Other study ID # UHN REB 04-0407-AE
Secondary ID
Status Recruiting
Phase Phase 4
First received September 13, 2005
Last updated June 11, 2007

Study information

Verified date September 2006
Source University Health Network, Toronto
Contact Peter Slinger, MD
Phone 416-340-5164
Email peter.slinger@uhn.on.ca
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Observational

Clinical Trial Summary

This is a clinical trial comparing surgical conditions during one-lung ventilation with three different bronchial blockers or with double-lumen endobronchial tubes.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 16 Years and older
Eligibility Inclusion Criteria:

- Left thoracotomy

Exclusion Criteria:

- Contraindication to lung isolation

Study Design

Allocation: Random Sample, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Locations

Country Name City State
Canada University Health Network Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
University Health Network, Toronto

Country where clinical trial is conducted

Canada, 

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