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Study group - MRI CO2 and O2 stress test for Delirium

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
able to provide informed consent
elective major surgery requiring a minimum stay of 2 days postoperatively
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 days
Awards & highlights

Study 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
  • Anesthesia Complications
  • Delirium

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

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

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Delirium
Secondary outcome measures
Length of Hospital stay

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
594 Previous Clinical Trials
199,430 Total Patients Enrolled
8 Trials studying Delirium
3,357 Patients Enrolled for Delirium

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~2 spots leftby Apr 2025