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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00468494
Other study ID # 0120060208
Secondary ID
Status Completed
Phase N/A
First received April 30, 2007
Last updated January 24, 2013
Start date September 2006
Est. completion date June 2010

Study information

Verified date January 2013
Source Rutgers, The State University of New Jersey
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 308
Est. completion date June 2010
Est. primary completion date June 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Elective surgery

- 18-80 years of age

Exclusion Criteria:

- Known diabetics

- Pregnant patients

- Cardiac surgery patients

- Liver transplant patients

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Medicine & Dentistry of New Jersey Newark New Jersey

Sponsors (1)

Lead Sponsor Collaborator
University of Medicine and Dentistry of New Jersey

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary glucose level at specific points Intraoperatively and in the PACU No
Secondary pt telephoned to assess for complications within 2 weeks of surgery No
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