Hyperinsulinemic Normoglycemic Clamp for Pancreas and Simultaneous Pancreas/Kidney Transplant Recipients
Primary Purpose
Postoperative Complications
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Hyperinsulinemic Normoglycemic Clamp
Sponsored by
About this trial
This is an interventional prevention trial for Postoperative Complications focused on measuring Pancreas Transplantation, Kidney Transplantation, Organ Transplantation, Pancreas and Simultaneous Pancreas/Kidney Transplant Recipients
Eligibility Criteria
Inclusion Criteria:
- Male or female patient over 18 years of age
- Patient is about to receive a pancreas or a simultaneous pancreas/kidney transplant
- Able to give written informed consent prior to any study specific procedure
Exclusion Criteria:
- Multi-organ transplant other than kidney transplant
- No central venous access available to deliver the D20W solution
Sites / Locations
- Hospital Royal VictoriaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Study Group
Control Group
Arm Description
Hyperinsulinemic Normoglycemic Clamp will be started at the time of surgery (before incision) and will be continue for 3 days.
Patients in the control group will receive standard care.
Outcomes
Primary Outcome Measures
The number of post-transplants all complications up to 30 days (Clavien grading).
Secondary Outcome Measures
The number of 30 days post-transplant serious medical complication (Clavien grade 3, 4)
The length of hospital stay (days)
Full Information
NCT ID
NCT01001273
First Posted
October 22, 2009
Last Updated
March 25, 2011
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
Collaborators
Astellas Pharma Canada, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT01001273
Brief Title
Hyperinsulinemic Normoglycemic Clamp for Pancreas and Simultaneous Pancreas/Kidney Transplant Recipients
Official Title
Hyperinsulinemic Normoglycemic Clamp for Pancreas and Simultaneous Pancreas/Kidney Transplant Recipients
Study Type
Interventional
2. Study Status
Record Verification Date
March 2011
Overall Recruitment Status
Unknown status
Study Start Date
April 2010 (undefined)
Primary Completion Date
April 2012 (Anticipated)
Study Completion Date
June 2012 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
Collaborators
Astellas Pharma Canada, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief 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%.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Complications
Keywords
Pancreas Transplantation, Kidney Transplantation, Organ Transplantation, Pancreas and Simultaneous Pancreas/Kidney Transplant Recipients
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Study Group
Arm Type
Experimental
Arm Description
Hyperinsulinemic Normoglycemic Clamp will be started at the time of surgery (before incision) and will be continue for 3 days.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Patients in the control group will receive standard care.
Intervention Type
Other
Intervention Name(s)
Hyperinsulinemic Normoglycemic Clamp
Intervention Description
The patient receives insulin intravenous infusion at 2ml units/kg/min. Dextrose 20% (D20W ®) will be titrated to maintain blood glucose between 4 - 6 mmol/L (72 - 108 mg/dl).
Primary Outcome Measure Information:
Title
The number of post-transplants all complications up to 30 days (Clavien grading).
Time Frame
30 days post-operative
Secondary Outcome Measure Information:
Title
The number of 30 days post-transplant serious medical complication (Clavien grade 3, 4)
Time Frame
30 days post-op
Title
The length of hospital stay (days)
Time Frame
Length of hospital stay (day 1 until discharge)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female patient over 18 years of age
Patient is about to receive a pancreas or a simultaneous pancreas/kidney transplant
Able to give written informed consent prior to any study specific procedure
Exclusion Criteria:
Multi-organ transplant other than kidney transplant
No central venous access available to deliver the D20W solution
Facility Information:
Facility Name
Hospital Royal Victoria
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3A1A1
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeanne M Bouteaud
Phone
514.934.1934
Ext
36237
Email
jeanne.bouteaud@muhc.mcgill.ca
First Name & Middle Initial & Last Name & Degree
Steven Paraskevas, MD, PhD
First Name & Middle Initial & Last Name & Degree
Mazen Hassanain, MD
First Name & Middle Initial & Last Name & Degree
Peter Metrakos, MD
First Name & Middle Initial & Last Name & Degree
Prosanto K Chaudhury, MD, Msc
First Name & Middle Initial & Last Name & Degree
Jean Tchervenkov, MD
First Name & Middle Initial & Last Name & Degree
Marcelo Cantarovitch, MD
First Name & Middle Initial & Last Name & Degree
George Carvalho, MD
First Name & Middle Initial & Last Name & Degree
Ralph Lattermann, MD
First Name & Middle Initial & Last Name & Degree
Thomas Schricker, MD
12. IPD Sharing Statement
Learn more about this trial
Hyperinsulinemic Normoglycemic Clamp for Pancreas and Simultaneous Pancreas/Kidney Transplant Recipients
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