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Perioperative Nutrition in Upper Gastrointestinal (GI) Cancer Surgery

Primary Purpose

Stomach Neoplasms, Esophageal Neoplasms

Status
Terminated
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Impact
Glucose load
Sponsored by
Dan Azagury
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stomach Neoplasms focused on measuring Gastric cancer, Esophageal cancer, Surgical complications, Immunonutrition

Eligibility Criteria

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

Inclusion Criteria:

  • Surgery for Upper GI cancer
  • Age over 18
  • Informed consent

Exclusion Criteria:

  • Major swallowing disorders
  • Dementia or other psychological state precluding compliance and understanding of research protocol
  • Pre-existing enteral or parenteral nutrition

Sites / Locations

  • Hôpitaux Universitaires Genève

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Nutrition

Control

Arm Description

Pre-operative immunonutritrion, pre-operative glucose load, post-operative early immunonutrition

No immunonutrition, no glucose load, no early enteral immunonutrition

Outcomes

Primary Outcome Measures

Rate of post-operative complications
Length of stay

Secondary Outcome Measures

Quality of life
Body composition

Full Information

First Posted
November 19, 2007
Last Updated
September 4, 2013
Sponsor
Dan Azagury
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1. Study Identification

Unique Protocol Identification Number
NCT00560846
Brief Title
Perioperative Nutrition in Upper Gastrointestinal (GI) Cancer Surgery
Official Title
Perioperative Nutrition in Upper GI Cancer Surgery (Oesophagectomy or Gastrectomy)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Terminated
Why Stopped
Insufficient recruitment over time.
Study Start Date
November 2007 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Dan Azagury

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to demonstrate the influence of peri-operative nutrition on the post-operative complications, preservation of lean body mass and length of stay after gastrectomy or oesophagectomy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stomach Neoplasms, Esophageal Neoplasms
Keywords
Gastric cancer, Esophageal cancer, Surgical complications, Immunonutrition

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
43 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Nutrition
Arm Type
Experimental
Arm Description
Pre-operative immunonutritrion, pre-operative glucose load, post-operative early immunonutrition
Arm Title
Control
Arm Type
No Intervention
Arm Description
No immunonutrition, no glucose load, no early enteral immunonutrition
Intervention Type
Dietary Supplement
Intervention Name(s)
Impact
Intervention Description
Preoperative 5 day oral Impact and early post-operative enteral Impact
Intervention Type
Dietary Supplement
Intervention Name(s)
Glucose load
Other Intervention Name(s)
PreOp Nutricia
Intervention Description
Pre-operative glucose load: 800 ml of PreOp (Nutricia) 12 h before surgery; 400 ml of PreOp (Nutricia) 2 hours before surgery
Primary Outcome Measure Information:
Title
Rate of post-operative complications
Time Frame
30 days
Title
Length of stay
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Quality of life
Time Frame
1 year
Title
Body composition
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Surgery for Upper GI cancer Age over 18 Informed consent Exclusion Criteria: Major swallowing disorders Dementia or other psychological state precluding compliance and understanding of research protocol Pre-existing enteral or parenteral nutrition
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dan E Azagury, MD
Organizational Affiliation
University Hospital, Geneva
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpitaux Universitaires Genève
City
Geneva
ZIP/Postal Code
1204
Country
Switzerland

12. IPD Sharing Statement

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Perioperative Nutrition in Upper Gastrointestinal (GI) Cancer Surgery

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