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

Sponsor
University Hospital Inselspital, Berne (Other)
Overall Status
Completed
CT.gov ID
NCT01552291
Collaborator
Fresenius Kabi (Industry)
42
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Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Glutamine
  • Drug: Placebo
Phase 4

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:
  1. Postoperative morbidity (surgical site infections, pneumonia, sepsis, incidence of wound and fascial dehiscence, incisional hernia, anastomotic break down)

  2. Nutritional status of the patients

  3. Postoperative cell damage and inflammatory response

  4. 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
42 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Supportive Care
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 Start Date :
May 1, 2012
Actual Primary Completion Date :
Feb 10, 2018
Actual Study Completion Date :
Feb 12, 2018

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Glutamin

Dietary Supplement: Glutamine
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

Placebo Comparator: Placebo

Drug: Placebo
30g oral maltodextrin / day for 5 days before surgery

Outcome Measures

Primary Outcome Measures

  1. Morbidity [6 weeks]

Secondary Outcome Measures

  1. Postoperative cell damage [Up to seven days after surgery]

  2. Inflammatory response [Up to seven days after surgery]

  3. Nutritional status [Up to seven days after surgery]

  4. Perioperative immunocompetence [Seven and one day(s) before surgery. Postoperative week 1 and 6.]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of visceral surgery and transplant surgery, Berne University Hospital Berne Switzerland 3010

Sponsors and Collaborators

  • University Hospital Inselspital, Berne
  • Fresenius Kabi

Investigators

  • Principal Investigator: Beat Schnüriger, PD Dr. med., Department of visceral surgery and transplant surgery, Berne University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital Inselspital, Berne
ClinicalTrials.gov Identifier:
NCT01552291
Other Study ID Numbers:
  • 170/11
First Posted:
Mar 13, 2012
Last Update Posted:
Feb 13, 2018
Last Verified:
Feb 1, 2018
Keywords provided by University Hospital Inselspital, Berne
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 13, 2018