- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00468494
Can Blood Glucose Levels During the Perioperative Period Identify a Population at Risk for Hyperglycemia?
January 24, 2013 updated by: University of Medicine and Dentistry of New Jersey
Can Blood Glucose Levels During the Perioperative Period Identify a Population at Risk for Hyperglycemia
Surgery performed during general anesthesia induces a stress effect on the body.
Our plan is to identify population at risk of hyperglycemia during perioperative period.
Study Overview
Status
Completed
Conditions
Detailed Description
This is a prospective study to define the relationship between time profile of glucose control before, during and after surgery with patient variables, surgical variables and anesthetic variables.
Serum glucose levels will be measured preoperatively and then at 30 minute intervals during surgery.
Pain score, pain medication and glucose levels will be measured in the post anesthesia recovery room.
Subjects will be contacted 2 weeks following the date of surgery to determine the incidence of postoperative complications.
Study Type
Observational
Enrollment (Actual)
308
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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New Jersey
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Newark, New Jersey, United States, 07101
- University of Medicine & Dentistry of New Jersey
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
non-diabetic adults undergoing surgery
Description
Inclusion Criteria:
- Elective surgery
- 18-80 years of age
Exclusion Criteria:
- Known diabetics
- Pregnant patients
- Cardiac surgery patients
- Liver transplant patients
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
glucose level at specific points
Time Frame: Intraoperatively and in the PACU
|
Intraoperatively and in the PACU
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
pt telephoned to assess for complications
Time Frame: within 2 weeks of surgery
|
within 2 weeks of surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Vasanti Tilak, MD, University of Medicine & Dentistry of New Jersey-NJMS
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2006
Primary Completion (Actual)
June 1, 2010
Study Completion (Actual)
June 1, 2010
Study Registration Dates
First Submitted
April 30, 2007
First Submitted That Met QC Criteria
May 1, 2007
First Posted (Estimate)
May 2, 2007
Study Record Updates
Last Update Posted (Estimate)
January 25, 2013
Last Update Submitted That Met QC Criteria
January 24, 2013
Last Verified
January 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0120060208
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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