Outcomes With Tight Control of Hyperglycemia in Cardiac Surgery Patients
Primary Purpose
Cardiac Surgical Procedures, Hyperglycemia
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Insulin infusion with a goal
Sponsored by
About this trial
This is an interventional treatment trial for Cardiac Surgical Procedures
Eligibility Criteria
Inclusion Criteria All subjects accepted for this study must be: >=18 years of age Undergoing an elective cardiac surgical procedure Exclusion Criteria Subjects who have one or more of the following will be excluded from the study: Undergoing surgery not utilizing cardiopulmonary bypass Unable to grant informed consent or comply with study procedure Undergoing emergency open heart-surgery 3. Are allergic to any of the excipients in insulin
Sites / Locations
- Mayo Clinic
Outcomes
Primary Outcome Measures
Mortality
Sternal wound infections
Stroke
Cardiac arrhythmias
Renal failure
Secondary Outcome Measures
Lenght of intensive care unit stay
Length of hospital stay
Safety of study insulin infusion
Efficacy of study insulin infusion
Full Information
NCT ID
NCT00282698
First Posted
January 26, 2006
Last Updated
May 20, 2011
Sponsor
Mayo Clinic
Collaborators
Novo Nordisk A/S
1. Study Identification
Unique Protocol Identification Number
NCT00282698
Brief Title
Outcomes With Tight Control of Hyperglycemia in Cardiac Surgery Patients
Official Title
Outcomes With Use Of Intensive Insulin Therapy In Intraoperative Management Of Hyperglycemia In Adult Patients Undergoing Cardiac Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
May 2011
Overall Recruitment Status
Completed
Study Start Date
July 2004 (undefined)
Primary Completion Date
May 2005 (Actual)
Study Completion Date
May 2005 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Mayo Clinic
Collaborators
Novo Nordisk A/S
4. Oversight
5. Study Description
Brief Summary
Patients with or without diabetes may have high blood sugar levels due to stress response of the body during heart surgery. This study is being done to determine if maintaining normal blood sugar levels during open-heart surgery by using intravenous insulin results in a lesser incidence of death, wound infections in the chest, disturbances of heart rhythm, kidney failure, stroke and prolonged time on the breathing machine (artificial ventilation) within 30 days after surgery.
Detailed Description
Rigorous intraoperative glycemic control may be of paramount importance in affecting outcomes after cardiac surgery. There is evidence that strict control of glucose levels postoperatively results in improved outcomes in patients undergoing cardiac surgery. There is currently no consensus on optimal management of hyperglycemia intraoperatively. The aim of this prospective randomized controlled clinical trial is to determine whether normalization of intraoperative glucose levels with insulin improves outcomes. The comparison group will be treated with current standard practice to control hyperglycemia during surgery. The primary outcome is a composite of mortality, sternal wound infections, prolonged pulmonary ventilation, cardiac arrhythmias (new-onset atrial fibrillation, heart block requiring permanent pacemaker, cardiac arrest), stroke and acute or worsening renal failure within 30 days after surgery. Secondary outcome measures are length of intensive care unit and hospital stay as well as safety and efficacy of the study insulin infusion protocol.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Surgical Procedures, Hyperglycemia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
400 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Insulin infusion with a goal
Primary Outcome Measure Information:
Title
Mortality
Title
Sternal wound infections
Title
Stroke
Title
Cardiac arrhythmias
Title
Renal failure
Secondary Outcome Measure Information:
Title
Lenght of intensive care unit stay
Title
Length of hospital stay
Title
Safety of study insulin infusion
Title
Efficacy of study insulin infusion
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria
All subjects accepted for this study must be:
>=18 years of age
Undergoing an elective cardiac surgical procedure
Exclusion Criteria
Subjects who have one or more of the following will be excluded from the study:
Undergoing surgery not utilizing cardiopulmonary bypass
Unable to grant informed consent or comply with study procedure
Undergoing emergency open heart-surgery
3. Are allergic to any of the excipients in insulin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gunjan Y. Gandhi, M.D.
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
17310047
Citation
Gandhi GY, Nuttall GA, Abel MD, Mullany CJ, Schaff HV, O'Brien PC, Johnson MG, Williams AR, Cutshall SM, Mundy LM, Rizza RA, McMahon MM. Intensive intraoperative insulin therapy versus conventional glucose management during cardiac surgery: a randomized trial. Ann Intern Med. 2007 Feb 20;146(4):233-43. doi: 10.7326/0003-4819-146-4-200702200-00002.
Results Reference
derived
Learn more about this trial
Outcomes With Tight Control of Hyperglycemia in Cardiac Surgery Patients
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