Modulating the Stress Response in Diabetes Mellitus Type 2 Patients Undergoing Colon Surgery

August 8, 2016 updated by: University Hospital, Basel, Switzerland

Background Surgical injury provokes a stress response. These pathways mediated by stress hormones and cytokines cause a catabolic state. The loss of body cell mass may result in prolonged convalescence and increased morbidity. Protein catabolism after colorectal surgery is even more increased in patients with type 2 diabetes mellitus. Epidural blockade, by reducing the intensity of the catabolic response, improves substrate utilization after surgery in non-diabetic patients. This effect is even more pronounced in diabetic patients receiving amino acids.

The aim of the study is to explore the effect of two different protocols to manage blood glucose control on glucose and protein metabolism in patients with type 2 diabetes mellitus undergoing colon surgery and receiving epidural analgesia and perioperative feeding with amino acids. The following hypotheses are tested:

  1. Tight perioperative blood glucose control with intensified insulin therapy compared to standard blood glucose control in presence of general anesthesia with epidural analgesia and amino acid infusion would reduce endogenous glucose production and leucine oxidation.
  2. Tight blood glucose control and perioperative infusion of amino acids induce a more positive protein balance compared to standard blood glucose control by better oxidative glucose utilization and redirecting amino acids from oxidative to synthetic pathways.

Material and Methods A total of 20 patients with diabetes mellitus type 2 undergoing elective colorectal surgery will be admitted to the study. Patients will be randomly assigned to receive standard blood glucose control (blood glucose target <10 mmol*l-1; control group; cytotoxic T lymphocyte (CTL) group, n=8) or to receive tight blood glucose control with intensified insulin therapy (blood glucose target<6 mmol*l-1; intensified insulin group; II group, n=8). All patients will receive general anesthesia and an epidural catheter for perioperative analgesia. During surgery (intraoperative state) and immediately after surgery (postoperative state) when receiving an amino acid infusion protein and glucose kinetics will be assessed using a stable isotope technique with L-[1-13C]leucine and [6,6-2H2]glucose and circulating concentrations of glucose, glucagon, insulin and cortisol will be measured. The primary endpoints of the study will be protein balance. Sample size is set to ensure at least 80% power at a significance level of 0.05.

Study Overview

Status

Completed

Detailed Description

see information below

Study Type

Interventional

Enrollment (Actual)

18

Phase

  • Not Applicable

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients undergoing elective colorectal surgery for non-metastatic disease
  • Type 2 diabetes mellitus with plasma level of glycosylated hemoglobin level (HbA(1c)) less than 10% indicating normal or moderate glycemic control
  • Being capable of signing informed consent
  • Accepting an epidural catheter for perioperative analgesia

Exclusion Criteria:

  • American Society of Anesthesiologists (ASA) Physical Status classification system 4 with major cardiac disorders (severe arrhythmias, recent myocardial ischemia (MI), heart failure, uncontrolled hypertension)
  • Hepatic disorders (liver failure, jaundice, metastatic disease), renal disorders (acute or chronic renal failure or on dialysis)
  • Metabolic disorders (untreated hyperthyroidism, pyrexia, more than 10% weight loss over the preceding three months, plasma albumin concentration < 35g/l)
  • Anemia (hemoglobin < 10 g/dl)
  • Chemotherapy or radiotherapy during six months before surgery
  • Inflammatory bowel disease or other inflammatory condition
  • Pregnancy
  • Previous spine surgery precluding placement of an epidural catheter.

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

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intensified insulin group
Patients undergoing elective colorectal surgery will receive standard anesthesia including epidural analgesia and nutritional support with an intravenous amino acid solution while receiving tight blood glucose control with intensified insulin therapy (blood glucose target<6 mmol*l-1) via an continuous insulin infusion.
Other Names:
  • continuous insulin infusion
No Intervention: Control group
Patients undergoing elective colorectal surgery will receive standard anesthesia including epidural analgesia and nutritional support with an intravenous amino acid solution while receiving standard blood glucose control (blood glucose target <10 mmol*l-1) via subcutaneous insulin boluses

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postoperative protein balance (leucine) (umol/kg/h)
Time Frame: Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Measured and calculated with a 3-hour stable isotope tracer technique with L-(1-13C)leucine and calorimetry towards the end of the 3 hour period
Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intraoperative protein metabolism: Rate of appearance of leucine (umol/kg/h)
Time Frame: Intraoperative period: starting with the induction of anesthesia and ending after 3 hours (during surgery)
Measured and calculated with a 3-hour stable isotope tracer technique with L-(1-13C)leucine
Intraoperative period: starting with the induction of anesthesia and ending after 3 hours (during surgery)
Intraoperative protein metabolism: endogenous rate of appearance of leucine (umol/kg/h)
Time Frame: Intraoperative period: starting with the induction of anesthesia and ending after 3 hours (during surgery)
Measured and calculated with a 3-hour stable isotope tracer technique with L-(1-13C)leucine
Intraoperative period: starting with the induction of anesthesia and ending after 3 hours (during surgery)
Intraoperative glucose metabolism: Endogenous rate of appearance of glucose (umol/kg/min)
Time Frame: Intraoperative period: starting with the induction of anesthesia and ending after 3 hours (during surgery)
Measured and calculated with a 3-hour stable isotope tracer technique with D-(6,6-2H2)glucose
Intraoperative period: starting with the induction of anesthesia and ending after 3 hours (during surgery)
Intraoperative glucose metabolism: Glucose clearance (ml/kg/min)
Time Frame: Intraoperative period: starting with the induction of anesthesia and ending after 3 hours (during surgery)
Measured and calculated with a 3-hour stable isotope tracer technique with D-(6,6-2H2)glucose and plasma glucose measurement
Intraoperative period: starting with the induction of anesthesia and ending after 3 hours (during surgery)
Postoperative protein metabolism: Rate of appearance of leucine (umol/kg/h)
Time Frame: Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Measured and calculated with a 3-hour stable isotope tracer technique with L-(1-13C)leucine and calorimetry towards the end of the 3 hour period
Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Postoperative protein metabolism: Endogenous rate of appearance of leucine (umol/kg/h)
Time Frame: Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Measured and calculated with a 3-hour stable isotope tracer technique with L-(1-13C)leucine and calorimetry towards the end of the 3 hour period
Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Postoperative protein metabolism: Leucine oxidation (umol/kg/h)
Time Frame: Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Measured and calculated with a 3-hour stable isotope tracer technique with L-(1-13C)leucine and calorimetry towards the end of the 3 hour period
Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Postoperative protein metabolism: Protein synthesis (leucine) (umol/kg/h)
Time Frame: Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Measured and calculated with a 3-hour stable isotope tracer technique with L-(1-13C)leucine and calorimetry towards the end of the 3 hour period
Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Postoperative glucose metabolism: Endogenous rate of appearance of glucose (umol/kg/min)
Time Frame: Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Measured and calculated with a 3-hour stable isotope tracer technique with D-(6,6-2H2)glucose
Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Postoperative glucose metabolism: Glucose clearance (ml/kg/min)
Time Frame: Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours
Measured and calculated with a 3-hour stable isotope tracer technique with D-(6,6-2H2)glucose and plasma glucose measurement
Postoperative period: starting with arrival in the postoperative care unit and ending after 3 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Andrea Kopp Lugli, MD, MSc, University Hospital, Basel, Switzerland

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

December 1, 2009

Primary Completion (Actual)

November 1, 2010

Study Completion (Actual)

November 1, 2010

Study Registration Dates

First Submitted

August 8, 2016

First Submitted That Met QC Criteria

August 8, 2016

First Posted (Estimate)

August 11, 2016

Study Record Updates

Last Update Posted (Estimate)

August 11, 2016

Last Update Submitted That Met QC Criteria

August 8, 2016

Last Verified

August 1, 2016

More Information

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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