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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
Mayo Clinic
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Surgical Procedures

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
January 26, 2006
Last Updated
May 20, 2011
Sponsor
Mayo Clinic
Collaborators
Novo Nordisk A/S
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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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