Efficiency of Two Glucose Sampling Protocols for Maintenance of Euglycemia
Primary Purpose
Brain Neoplasms, Intracranial Aneurysm
Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Insulin
Sponsored by
About this trial
This is an interventional treatment trial for Brain Neoplasms focused on measuring Euglycemia, craniotomy, neurosurgery, hypoglycemia, insulin
Eligibility Criteria
Inclusion Criteria:
- All English speaking, non-diabetic, non-pregnant patients over the age of 18 undergoing open craniotomy for the surgical treatment of tumors or intracranial aneurysms.
Exclusion Criteria:
- Patients under 18 years of age, patients who are pregnant, patients with diabetes, BMI > 33 kg/m2.
Sites / Locations
- Dhanesh Gupta
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Q1 hour protocol
Q30min protocol
Arm Description
change of insulin infusion every hour
change of insulin infusion every 30 minutes
Outcomes
Primary Outcome Measures
performance of each of glucose sampling and insulin protocols for achieving euglycemia
performance of each of glucose sampling and insulin protocols for achieving euglycemia during the operation
Secondary Outcome Measures
hypoglycemia
Hypoglycemia occurring the operation
time required to reach euglycemia
Elapsed time required to reach euglycemia during the operation
relationship of BMI and performance of protocols
Evaluating the relationship of BMI (Body Mass Index) and the performance of protocols during the operation
relationship of serum biomarkers of insulin resistance and performance of protocols
Evaluating the relationship of serum biomarkers of insulin resistance and performance of protocols during the operation
Full Information
NCT ID
NCT00993057
First Posted
October 8, 2009
Last Updated
December 11, 2019
Sponsor
Northwestern University
1. Study Identification
Unique Protocol Identification Number
NCT00993057
Brief Title
Efficiency of Two Glucose Sampling Protocols for Maintenance of Euglycemia
Official Title
Comparing Two Glucose Sampling Frequencies for an Intensive Insulin Protocol During Craniotomy in Non-Diabetic Patients-How Efficiently and Safely Can We Maintain Target Glucose Levels
Study Type
Interventional
2. Study Status
Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
What is the efficacy and safety of q 30 minutes vs. q 1hour glucose sampling and intervention for an intensive insulin protocol to achieve and maintain euglycemia in non-diabetic patients undergoing craniotomy? The investigators hypothesize that in non-diabetic patients undergoing craniotomy, monitoring glucose and modifying insulin infusions every 30 minutes compared to every hour will help them reach target glucose levels faster and maintain them more efficiently with the same insulin protocol.
Detailed Description
Intraoperative blood glucose levels will be maintained in the target range of 90-110 mg/dL (euglycemia) using the protocol. The target serum glucose ranges chosen (90-110 mg/dL) was chosen to specifically target those levels associated with the best outcome in cerebral aneurysm surgery (serum glucose < 108 mg/dL) and aggressively avoid those levels associated with cognitive dysfunction (serum glucose < 128 mg/dL) and gross neurologic deficits (serum glucose < 152 mg/dL). Because the strength of these data, the investigators utilize an aggressive insulin protocol in their routine clinical care of patients undergoing craniotomies.
Each patient will be randomly assigned to one of two frequency of intervention groups-Group 30 will have the insulin dose adjusted every 30 minutes and Group 60 will have the insulin dose adjusted every 60 minutes. Blood glucose levels, insulin boluses and infusion rates, and dextrose boluses will be recorded on the respective Intraoperative Insulin & Glucose data sheet (Appendix 2 and 3 for Group 30 and Group 60, respectively).
Regardless of the protocol, glucose measurements will be conducted every 15 minutes but insulin intervention will be done at 30 minutes or one hour (per assigned treatment group). The interval data (15 minutes for the 30 min group and 15, 30, and 45 minutes for the 1 hour group) will be utilized to determine the pharmacodynamic effects of insulin (dose-response relationship). Interventions will only be performed at the assigned interval (30 vs 60 min) unless the glucose level is < 70 mg/dL, at which time the patient will receive 25 mL of 50% Dextrose solution. For these rescued patients, the protocol will be continued as scheduled.
On the day of surgery, after confirming entry into the study (i.e., confirmation of research consent), each patient will be randomly assigned to a specific protocol-q 30 minutes glucose measurements and intervention vs. q 60 minutes glucose measurements and intervention.Randomization will be performed in blocks of 10 using a computer generated random number assignment (odd numbers = q 30 minutes and even numbers = q 60 minutes)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Neoplasms, Intracranial Aneurysm
Keywords
Euglycemia, craniotomy, neurosurgery, hypoglycemia, insulin
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Q1 hour protocol
Arm Type
Active Comparator
Arm Description
change of insulin infusion every hour
Arm Title
Q30min protocol
Arm Type
Active Comparator
Arm Description
change of insulin infusion every 30 minutes
Intervention Type
Drug
Intervention Name(s)
Insulin
Other Intervention Name(s)
Humulin
Intervention Description
Adjustable insulin infusion scale with loading doses
Primary Outcome Measure Information:
Title
performance of each of glucose sampling and insulin protocols for achieving euglycemia
Description
performance of each of glucose sampling and insulin protocols for achieving euglycemia during the operation
Time Frame
duration of operation
Secondary Outcome Measure Information:
Title
hypoglycemia
Description
Hypoglycemia occurring the operation
Time Frame
duration of operation
Title
time required to reach euglycemia
Description
Elapsed time required to reach euglycemia during the operation
Time Frame
durarion of operation
Title
relationship of BMI and performance of protocols
Description
Evaluating the relationship of BMI (Body Mass Index) and the performance of protocols during the operation
Time Frame
duration of operation
Title
relationship of serum biomarkers of insulin resistance and performance of protocols
Description
Evaluating the relationship of serum biomarkers of insulin resistance and performance of protocols during the operation
Time Frame
duration of operation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All English speaking, non-diabetic, non-pregnant patients over the age of 18 undergoing open craniotomy for the surgical treatment of tumors or intracranial aneurysms.
Exclusion Criteria:
Patients under 18 years of age, patients who are pregnant, patients with diabetes, BMI > 33 kg/m2.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dhanesh Gupta, MD
Organizational Affiliation
Northwestern University Feinberg School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dhanesh Gupta
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Efficiency of Two Glucose Sampling Protocols for Maintenance of Euglycemia
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