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Air/Oxygen Mixture for Pulmonary Atelectasis
N/A
Waitlist Available
Led By Neal Badner, MD, FRCP(C)
Research Sponsored by London Health Sciences Centre
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up intra-operative and post operative day 1 and 2 .
Awards & highlights
Study Summary
Patients scheduled for lung lobe resection using video assisted thoracic surgery will be randomly assigned to be ventilated with either only oxygen or a mixture of air and oxygen. The primary purpose of this study is to determine if the incidence of postoperative collapse (in the non-surgical lung) is decreased when using a mixture of air and oxygen compared to using only oxygen (which is our control measurement) during one-lung ventilation.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ intra-operative and post operative day 1 and 2 .
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~intra-operative and post operative day 1 and 2 .
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
The incidence of postoperative atelectasis
Secondary outcome measures
The incidence of intraoperative and postoperative hypoxia (SpO2 < 90%) .
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Air/Oxygen MixtureExperimental Treatment1 Intervention
Patients in this group will be ventilated with a mixture of air and oxygen during one lung ventilation.
Group II: OxygenActive Control1 Intervention
Patients in this group will be ventilated with only oxygen during one lung ventilation.
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Who is running the clinical trial?
London Health Sciences CentreLead Sponsor
143 Previous Clinical Trials
49,892 Total Patients Enrolled
Neal Badner, MD, FRCP(C)Principal InvestigatorLondon Health Science Centre, University Of Western Ontario
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