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Study Group for Postoperative Complications
N/A
Waitlist Available
Research Sponsored by McGill University Health Centre/Research Institute of the McGill University Health 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 30 days post-op
Awards & highlights
Study Summary
This study proposes a simple and safe way of lowering this complicate rate, while improving graft recovering and protecting the graft as it recovers from the transplant. The investigators hypothesize that by maintaining a tight glucose control via a glucose-insulin clamp during surgery and 72 hours post-operatively the investigators will be able to lower the complication rate by 50%.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 30 days post-op
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days post-op
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
The number of post-transplants all complications up to 30 days (Clavien grading).
Secondary outcome measures
The length of hospital stay (days)
The number of 30 days post-transplant serious medical complication (Clavien grade 3, 4)
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Study GroupExperimental Treatment1 Intervention
Hyperinsulinemic Normoglycemic Clamp will be started at the time of surgery (before incision) and will be continue for 3 days.
Group II: Control GroupActive Control1 Intervention
Patients in the control group will receive standard care.
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Who is running the clinical trial?
McGill University Health Centre/Research Institute of the McGill University Health CentreLead Sponsor
442 Previous Clinical Trials
159,094 Total Patients Enrolled
1 Trials studying Postoperative Complications
318 Patients Enrolled for Postoperative Complications
Astellas Pharma Canada, Inc.Industry Sponsor
23 Previous Clinical Trials
3,518 Total Patients Enrolled
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