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The Impact of Preoperative Oral Glutamine Intake on the Immunocompetence and Outcomes of Malnourished Patients Undergoing Major Abdominal Surgery Due to Malignancies (Glutaminprojec)

Primary Purpose

Malnourishment, Gastrointestinal Tumors

Status
Completed
Phase
Phase 4
Locations
Switzerland
Study Type
Interventional
Intervention
Glutamine
Placebo
Sponsored by
Insel Gruppe AG, University Hospital Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Malnourishment focused on measuring Malnourishment, Gastrointestinal tumors, Immunocompetence

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically confirmed and surgically resectable carcinomas
  • Candidates for elective surgery with an estimated surgical stress score
  • A Nutritional Risk Screening 2002 (NRS-200232) score ≥3
  • Age ≥ 18 years
  • Completed primary immunization with tetanus toxoid
  • Last tetanus booster ≥10 years back
  • Informed consent

Exclusion Criteria

  • Refusal to participate
  • Clinically relevant alterations of the pulmonary renal of hepatic function
  • Insulin-dependent diabetes mellitus
  • Pre-existing autoimmune diseases and immune-deficiencies
  • Neutropenia
  • Pregnancy
  • Age <18 years
  • Last tetanus booster <10 years back
  • Ongoing infection
  • Intestinal obstruction at the time of entry into the study

Sites / Locations

  • Department of visceral surgery and transplant surgery, Berne University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Glutamin

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Morbidity

Secondary Outcome Measures

Postoperative cell damage
Inflammatory response
Nutritional status
Perioperative immunocompetence

Full Information

First Posted
March 5, 2012
Last Updated
February 12, 2018
Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
Fresenius Kabi
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1. Study Identification

Unique Protocol Identification Number
NCT01552291
Brief Title
The Impact of Preoperative Oral Glutamine Intake on the Immunocompetence and Outcomes of Malnourished Patients Undergoing Major Abdominal Surgery Due to Malignancies
Acronym
Glutaminprojec
Official Title
The Impact of Preoperative Oral Glutamine Intake on the Immunocompetence and Outcomes of Malnourished Patients Undergoing Major Abdominal Surgery Due to Malignancies - A Randomized, Placebo-controlled Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
February 10, 2018 (Actual)
Study Completion Date
February 12, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
Fresenius Kabi

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Malnutrition occurs in up to 50% of patients requiring elective surgery for neoplastic diseases. It exerts a detrimental influence on outcome of surgery, because it can suppress immune function, exaggerate stress response and cause organ system dysfunction. Increased susceptibility to infection, protracted wound healing, impaired blood clotting and vessel wall fragility have been shown to be the leading causes of postoperative morbidity and mortality in malnourished patients undergoing major surgical resections. This trial is designed as a prospective randomized, double-blinded, placebo-controlled pilot study in a academic single center in Switzerland. A total of 50 malnourished patients with gastro-intestinal tumors will receive orally glutamine or placebo-treatment during a period of 5 days prior to surgery. The investigators hypothesize that oral Glutamine administration is feasible, well tolerated, will decrease postoperative morbidity, will suppress postoperative cell damage and inflammatory response, and will improve the perioperative immunocompetence of the patients.
Detailed Description
Background Malnutrition occurs in up to 50% of patients requiring elective surgery for neoplastic diseases. It exerts a detrimental influence on outcome of surgery, because it can suppress immune function, exaggerate stress response and cause organ system dysfunction. Increased susceptibility to infection, protracted wound healing, impaired blood clotting and vessel wall fragility have been shown to be the leading causes of postoperative morbidity and mortality in malnourished patients undergoing major surgical resections. Immuno- or pharmaconutrition, defined as enteral or parenteral nutritional therapy based on a variety of products, such as omega-3-fatty acids, glutamine, arginine, sulfur-containing amino acids, nucleotides and anti-oxidants, is thought to have beneficial effects on postoperative recovery in a wide variety of surgical patients. Studies have shown its clinical effectiveness in terms of reduced postoperative complications, shortening the hospital stay and reduced hospitalization costs. Torosian et al. showed that severely malnourished patients benefit from preoperative nutrition, which reduce postoperative complications by 20%. Although there is clinical evidence for the administration of immunonutrition to patients in the perioperative period, our understanding of the optimal type and time of immunonutrition, the characteristics of patients that benefit most, as well as the immunological mechanisms responsible for its beneficial effect is limited. Objective To assess in malnourished cancer patients the effect of 30g oral glutamine/day (3 sachets KABI® glutamine, Fresenius Kabi/day) for a preoperative course of 5 days on: Postoperative morbidity (surgical site infections, pneumonia, sepsis, incidence of wound and fascial dehiscence, incisional hernia, anastomotic break down) Nutritional status of the patients Postoperative cell damage and inflammatory response Perioperative immunocompetence Methods Seven days before surgery, the patients will receive a tetanus booster shot and will be randomly enrolled in either the 'glutamine group' or into the 'placebo group'. The patients as well as the responsible surgeons will be blinded. Patients in the 'glutamine group' will receive 30g oral glutamine / day for 5 days before surgery. Patients in the 'control group' will receive 30g oral maltodextrin / day for 5 days before surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnourishment, Gastrointestinal Tumors
Keywords
Malnourishment, Gastrointestinal tumors, Immunocompetence

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Glutamin
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Glutamine
Intervention Description
30g oral glutamine / day for 5 days before surgery. Glutamine is an important nonessential amino acid and its intracellular concentration is much higher than that of other amino acids. Glutamine is released in large quantities from skeletal muscle and serves as an important carrier and donor of nitrogen
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
30g oral maltodextrin / day for 5 days before surgery
Primary Outcome Measure Information:
Title
Morbidity
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Postoperative cell damage
Time Frame
Up to seven days after surgery
Title
Inflammatory response
Time Frame
Up to seven days after surgery
Title
Nutritional status
Time Frame
Up to seven days after surgery
Title
Perioperative immunocompetence
Time Frame
Seven and one day(s) before surgery. Postoperative week 1 and 6.

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed and surgically resectable carcinomas Candidates for elective surgery with an estimated surgical stress score A Nutritional Risk Screening 2002 (NRS-200232) score ≥3 Age ≥ 18 years Completed primary immunization with tetanus toxoid Last tetanus booster ≥10 years back Informed consent Exclusion Criteria Refusal to participate Clinically relevant alterations of the pulmonary renal of hepatic function Insulin-dependent diabetes mellitus Pre-existing autoimmune diseases and immune-deficiencies Neutropenia Pregnancy Age <18 years Last tetanus booster <10 years back Ongoing infection Intestinal obstruction at the time of entry into the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Beat Schnüriger, PD Dr. med.
Organizational Affiliation
Department of visceral surgery and transplant surgery, Berne University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of visceral surgery and transplant surgery, Berne University Hospital
City
Berne
ZIP/Postal Code
3010
Country
Switzerland

12. IPD Sharing Statement

Learn more about this trial

The Impact of Preoperative Oral Glutamine Intake on the Immunocompetence and Outcomes of Malnourished Patients Undergoing Major Abdominal Surgery Due to Malignancies

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