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Tight End-tidal Gas Control During Anesthesia to Decrease Postoperative Delirium Anesthetic Management
N/A
Waitlist Available
Research Sponsored by University of Manitoba
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 5 days
Awards & highlights
No Placebo-Only Group
Summary
This trial will study whether tight control of oxygen and carbon dioxide levels during anesthesia can decrease the incidence of postoperative delirium.
Eligible Conditions
- Delirium
- Anesthesia Complications
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ time (days) from admission to discharge from hospital (or through study completion at one year)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~time (days) from admission to discharge from hospital (or through study completion at one year)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Delirium
Secondary study objectives
Length of Hospital stay
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Study group - MRI CO2 and O2 stress testExperimental Treatment1 Intervention
Pilot Study of Feasibility of tight control of end-tidal respiratory gases during conduct of anesthesia
Find a Location
Who is running the clinical trial?
University of ManitobaLead Sponsor
621 Previous Clinical Trials
206,551 Total Patients Enrolled
8 Trials studying Delirium
3,303 Patients Enrolled for Delirium