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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 weeks
Treatment ~ Varies
Follow Up ~time (days) from admission to discharge from hospital (or through study completion at one year)
This trial's timeline: 3 weeks for screening, Varies for treatment, and time (days) from admission to discharge from hospital (or through study completion at one year) for reporting.

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
~2 spots leftby Dec 2025