search
Back to results

Dipeptide Alanyl Glutamine and Postoperative Insulin Resistance in Colon Carcinoma Patients (AIRCo)

Primary Purpose

Colon Carcinoma

Status
Unknown status
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Dipeptide Alanyl-Glutamine
Placebo
Dipeptide Alanyl-Glutamine
Sponsored by
Medical Center Alkmaar
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colon Carcinoma focused on measuring Dipeptide Alanyl-Glutamine, Insulin sensitivity, Intracellular signaling, Antioxidant/oxidant parameters, Lipolysis, Inflammatory response in the liver

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age between 18 and 75 years
  • Colon cancer patients scheduled for elective open abdominal surgery
  • Capable of giving informed consent

Exclusion Criteria:

  • Patients who are participating in another clinical trial
  • Unable to receive oral intake
  • Major malabsorption disorder of the gut
  • Patients with diabetes mellitus
  • BMI above 30 kg/m2
  • Use of certain medication: thyroid medication, corticosteroids, diuretic medication
  • Known bleeding disorders or increased PTT and or APTT
  • Any medical condition except for colon cancer

Sites / Locations

  • Medical Center AlkmaarRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Placebo Comparator

Active Comparator

Arm Label

Dipeptiven Arm Enteral

Placebo Arm Enteral and Intravenously

Dipeptiven ARM Intravenously

Arm Description

Outcomes

Primary Outcome Measures

The effect of intravenously and enterally administered dipeptide alanyl-glutamine preoperatively on postoperative insulin resistance in colon cancer patients.given, on postoperative insulin resistance in colon cancer patients.

Secondary Outcome Measures

The effect of the dipeptide alanyl-glutamine on components of the insulin signalling cascade in muscle tissue.
The effect of the dipeptide alanyl-glutamine on the systemic inflammatory response as well as on inflammatory pathways in muscle.
The effect of the dipeptide alanyl-glutamine on the amino acid concentration in muscle tissue.
The effect of the dipeptide alanyl-glutamine on antioxidant/oxidant parameters in the circulating compartment.
The effect of dipeptide alanyl-glutamine on the inflammatory response in the liver
The effect of dipeptide alanyl-glutamine on lipolysis.
The effect of dipeptide alanyl-glutamine on key enzymes involved in glucose production.

Full Information

First Posted
June 16, 2009
Last Updated
July 20, 2011
Sponsor
Medical Center Alkmaar
search

1. Study Identification

Unique Protocol Identification Number
NCT00922688
Brief Title
Dipeptide Alanyl Glutamine and Postoperative Insulin Resistance in Colon Carcinoma Patients
Acronym
AIRCo
Official Title
Dipeptide Alanyl Glutamine and Postoperative Insulin Resistance in Colon Carcinoma Patients
Study Type
Interventional

2. Study Status

Record Verification Date
November 2010
Overall Recruitment Status
Unknown status
Study Start Date
December 2010 (undefined)
Primary Completion Date
December 2012 (Anticipated)
Study Completion Date
May 2013 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Medical Center Alkmaar

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Rationale: It is well known that insulin resistance occurs after mediocre and intensive surgery, such as colon cancer surgery. Disturbances in insulin action negatively affect the postoperative recovery, either by prolonging the capacity of the body to regain normal function, or by increasing the metabolic stress and the risk for complications. Several studies have shown that focusing therapies on improving insulin resistance is successful. Experimental studies have shown that antioxidant agents, like glutamine (a precursor of glutathione), improve insulin sensitivity. The hypothesis of this study is that perioperative parenteral or enteral administration of glutamine, given as the dipeptide alanyl-glutamine, will reduce or prevent postoperative insulin resistance in colon cancer patients. The study will also be focused on the different routes of administration, because of the expected differential metabolic effects. Objective: The investigators' primary objective is to study whether intravenous or enteral administration of the dipeptide alanyl-glutamine will reduce or prevent postoperative insulin resistance in colon cancer patients. Study design: A double-blinded, placebo controlled randomised, pilot study at the Surgery Department of the Medical Center Alkmaar. Study population: Thirty patients of male gender and any ethnicity, who will undergo elective open abdominal colon surgery for colon cancer, aged 18-75 years. Intervention: Patients will receive dipeptide alanyl-glutamine intravenously or enterally, starting 24 hours prior to surgery, until 24 hours after surgery in the dosage of 0.5 g/kg/day, or saline (control group), for the same period of time. Main study parameters/endpoints: The main study parameter is postoperative insulin resistance. Secondary study parameters are lipolysis, oxidative stress and glucoregulatory hormones. Muscle, liver and fat biopsies will be taken to study insulin sensitive as well as inflammatory pathways.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Carcinoma
Keywords
Dipeptide Alanyl-Glutamine, Insulin sensitivity, Intracellular signaling, Antioxidant/oxidant parameters, Lipolysis, Inflammatory response in the liver

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Dipeptiven Arm Enteral
Arm Type
Active Comparator
Arm Title
Placebo Arm Enteral and Intravenously
Arm Type
Placebo Comparator
Arm Title
Dipeptiven ARM Intravenously
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Dipeptide Alanyl-Glutamine
Intervention Description
Intravenous supplementation of the dipeptide alanyl-glutamine is started 24 hours prior to surgery (dosage glutamine: 0,5 g/kg/day, and continued 24 hours postoperatively.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Intravenous and enteral supplementation of placebo is started 24 hours prior to surgery and continued 24 hours postoperatively.
Intervention Type
Drug
Intervention Name(s)
Dipeptide Alanyl-Glutamine
Intervention Description
Enteral supplementation of the dipeptide alanyl-glutamine is started 24 hours prior to surgery (dosage glutamine: 0,5 g/kg/day, and continued 24 hours postoperatively.
Primary Outcome Measure Information:
Title
The effect of intravenously and enterally administered dipeptide alanyl-glutamine preoperatively on postoperative insulin resistance in colon cancer patients.given, on postoperative insulin resistance in colon cancer patients.
Time Frame
Before and 1 day after surgery
Secondary Outcome Measure Information:
Title
The effect of the dipeptide alanyl-glutamine on components of the insulin signalling cascade in muscle tissue.
Time Frame
Before and 1 day after surgery
Title
The effect of the dipeptide alanyl-glutamine on the systemic inflammatory response as well as on inflammatory pathways in muscle.
Time Frame
Before and 1 day after surgery
Title
The effect of the dipeptide alanyl-glutamine on the amino acid concentration in muscle tissue.
Time Frame
Before and 1 day after surgery
Title
The effect of the dipeptide alanyl-glutamine on antioxidant/oxidant parameters in the circulating compartment.
Time Frame
Before and 1 day after surgery
Title
The effect of dipeptide alanyl-glutamine on the inflammatory response in the liver
Time Frame
During surgery
Title
The effect of dipeptide alanyl-glutamine on lipolysis.
Time Frame
Before and 1 day after surgery
Title
The effect of dipeptide alanyl-glutamine on key enzymes involved in glucose production.
Time Frame
Before and 1 day after surgery

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18 and 75 years Colon cancer patients scheduled for elective open abdominal surgery Capable of giving informed consent Exclusion Criteria: Patients who are participating in another clinical trial Unable to receive oral intake Major malabsorption disorder of the gut Patients with diabetes mellitus BMI above 30 kg/m2 Use of certain medication: thyroid medication, corticosteroids, diuretic medication Known bleeding disorders or increased PTT and or APTT Any medical condition except for colon cancer
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hamit Cakir, MD
Phone
0031725484444
Email
h.cakir@mca.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexander PJ Houdijk, MD,PhD
Organizational Affiliation
MCA Alkmaar
Official's Role
Study Director
Facility Information:
Facility Name
Medical Center Alkmaar
City
Alkmaar
State/Province
Noord holland
ZIP/Postal Code
1815 JD
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hamit Cakir, MD
Phone
0031725484444
Email
h.cakir@mca.nl
First Name & Middle Initial & Last Name & Degree
Alexander PJ Houdijk, MD, PhD
First Name & Middle Initial & Last Name & Degree
Hamit Cakir, MD

12. IPD Sharing Statement

Learn more about this trial

Dipeptide Alanyl Glutamine and Postoperative Insulin Resistance in Colon Carcinoma Patients

We'll reach out to this number within 24 hrs