Effect of Enteral Immunonutrition on Immune, Inflammatory Markers and Nutritional Status in Patients Undergoing Gastrectomy for Gastric Cancer
Primary Purpose
Gastric Cancer, Enteral Immunonutrition
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
enteral immunonutrition
Sponsored by
About this trial
This is an interventional supportive care trial for Gastric Cancer focused on measuring gastric cancer, enteral nutrition, enteral immunonutrition, immune function, inflammation response
Eligibility Criteria
Inclusion Criteria:
- Patients aged 18 to 80 years
- with histologically diagnosed cancer of stomach
- candidates for elective subtotal or total gastrectomy
Exclusion Criteria:
- pregnant or lactating woman,
- diagnoses of mental diseases
- resent severe concomitant diseases (chronic cardiopulmonary disease, chronic renal failure, etc.)
- known allergies to nutrition formula or component
- drug intolerance
- known immunodeficiency or autoimmune diseases
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
EIN group
SEN group
Arm Description
Enteral formula including not only basic energy components, but also immune components such as omega-3 fatty acids, glutamine (Gln), arginine (Arg), and nucleotide.
Enteral formula including only basic energy components.
Outcomes
Primary Outcome Measures
Change from baseline serum level of immune cytokines to postoperative day 5
levels of IgA, IgG and IgM in g/L,
Change from baseline serum level of immune markers to postoperative day 5
count of CD4+/CD8+
Change from baseline serum concentration of immune markers to postoperative day 5
percentage of CD3+ T cell of serum
Secondary Outcome Measures
changes among baseline, postoperative day 1, 3 and 5 serum concentration of inflammatory markers
concentration of white blood cell (WBC), C-reactive protein (CRP), interleukin-6 (IL-6) in g/L, and levels of tumor necrosis factor-α (TNF-α) in ng/L
Change among baseline, postoperative day 3 and 5 serum nutritional markers
concentration of albumin, prealbumin, and transferrin in g/L
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03730545
Brief Title
Effect of Enteral Immunonutrition on Immune, Inflammatory Markers and Nutritional Status in Patients Undergoing Gastrectomy for Gastric Cancer
Official Title
Effect of Enteral Immunonutrition on Immune, Inflammatory Markers and Nutritional Status in Patients Undergoing Gastrectomy for Gastric Cancer:a Randomized Double Blinded Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
January 1, 2017 (Actual)
Primary Completion Date
July 1, 2018 (Actual)
Study Completion Date
September 20, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
West China Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief Summary
Enteral immunonutrition (EIN) has been gaining increasing attention, but data of its immune and anti-inflammatory function in patients undergoing gastrectomy for gastric cancer are poorly investigated. The aim of this study was to assess the effect of EIN on immune function, inflammation response and nutrition status when compared to standard enteral nutrition (SEN).
The investigators believe that the proportion of cluster of differentiation 4 T-cells(CD4+T-cells), cluster of differentiation 3 T-cells(CD3+T-cells) and the counts of CD4+ / cluster of differentiation 8 T-cells (CD8+), immunoglobulin G(IgG), immunoglobulin M(IgM), and immunoglobulin A (IgA) were larger in EIN group, while the level of WBC, CRP and TNF-α were lower and nutritional status was similar.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer, Enteral Immunonutrition
Keywords
gastric cancer, enteral nutrition, enteral immunonutrition, immune function, inflammation response
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients were randomized to receive enteral immunonutrition or standard enteral nutrition in postoperative day 1 by enteral feeding.
Masking
ParticipantInvestigator
Masking Description
Eligible patients were randomly assigned in equal numbers to undergo SEN or EIN according to a computer-generated randomization list managed by a dietary nurse not involved in the study. The study was double-blind: SEN and EIN feeds were identical in color and type of container, so treatment assignments were not revealed to patients or to any staff members.
Allocation
Randomized
Enrollment
124 (Actual)
8. Arms, Groups, and Interventions
Arm Title
EIN group
Arm Type
Experimental
Arm Description
Enteral formula including not only basic energy components, but also immune components such as omega-3 fatty acids, glutamine (Gln), arginine (Arg), and nucleotide.
Arm Title
SEN group
Arm Type
Active Comparator
Arm Description
Enteral formula including only basic energy components.
Intervention Type
Dietary Supplement
Intervention Name(s)
enteral immunonutrition
Intervention Description
Enteral nutrition was started within 12h at an infusion rate of 20ml per hour for SEN group and 16ml per hour for EIN group in the first 24h. The rates of flow were gradually increasing with 50ml/h in SEN versus 40ml/h in EIN on day 2, 70ml/h versus 56ml/h on day 3 and 100ml/h versus 80ml/h until the 7th day depending on the feeding tolerance.
Primary Outcome Measure Information:
Title
Change from baseline serum level of immune cytokines to postoperative day 5
Description
levels of IgA, IgG and IgM in g/L,
Time Frame
baseline and postoperative day 5
Title
Change from baseline serum level of immune markers to postoperative day 5
Description
count of CD4+/CD8+
Time Frame
baseline, postoperative day 5(POD 5)
Title
Change from baseline serum concentration of immune markers to postoperative day 5
Description
percentage of CD3+ T cell of serum
Time Frame
baseline, postoperative day 5(POD 5)
Secondary Outcome Measure Information:
Title
changes among baseline, postoperative day 1, 3 and 5 serum concentration of inflammatory markers
Description
concentration of white blood cell (WBC), C-reactive protein (CRP), interleukin-6 (IL-6) in g/L, and levels of tumor necrosis factor-α (TNF-α) in ng/L
Time Frame
baseline, postoperative day 1, 3, and 5
Title
Change among baseline, postoperative day 3 and 5 serum nutritional markers
Description
concentration of albumin, prealbumin, and transferrin in g/L
Time Frame
baseline,postoperative day 3 and 5
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients aged 18 to 80 years
with histologically diagnosed cancer of stomach
candidates for elective subtotal or total gastrectomy
Exclusion Criteria:
pregnant or lactating woman,
diagnoses of mental diseases
resent severe concomitant diseases (chronic cardiopulmonary disease, chronic renal failure, etc.)
known allergies to nutrition formula or component
drug intolerance
known immunodeficiency or autoimmune diseases
12. IPD Sharing Statement
Learn more about this trial
Effect of Enteral Immunonutrition on Immune, Inflammatory Markers and Nutritional Status in Patients Undergoing Gastrectomy for Gastric Cancer
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