Evaluation of Endobronchial Ultrasound (EBUS) for Staging Lung Cancer
NCT ID: NCT01799980
Last Updated: 2019-03-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
37 participants
OBSERVATIONAL
2012-06-30
2018-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Cervical mediastinoscopy
This group will undergo cervical mediastinoscopy before surgery to stage their lung cancer (procedure decided by the surgeon).
No interventions assigned to this group
Endo-bronchial ultrasound
This group will undergo endobronchial ultrasound before surgery to stage their lung cancer (procedure decided by the surgeon).
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Gender- Males and Female
Diagnosis of Non Small Cell Lung Cancer.
Patients who have consented on an Ottawa Hospital consent form to undergo a mediastinoscopy procedure or EBUS-TBNA, and a Positron emission tomography (PET) of the chest for lung cancer staging.
Exclusion Criteria
Patients who do not provide their Ottawa Hospital consent to undergo a staging bronchoscopy , cervical mediastinoscopy or EBUS-TBNA.
18 Years
ALL
No
Sponsors
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Ottawa Hospital Research Institute
OTHER
Responsible Party
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Principal Investigators
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Donna E Maziak, MD, MSc
Role: PRINCIPAL_INVESTIGATOR
Ottawa Hospital Research Institute
Locations
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Ottawa Hospital Research Institute
Ottawa, Ontario, Canada
Countries
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Other Identifiers
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2009471-01H
Identifier Type: -
Identifier Source: org_study_id
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