Trial on Impact on the Hospital Stay, of an Early Oral Nutrition Protocol Applied to Patients After Total Gastrectomy. (DOPGT_2015)

February 16, 2021 updated by: Leandre Farran Teixidor, Hospital Universitari de Bellvitge

Impact on the Hospital Stay, of an Early Oral Nutrition Protocol Applied to Gastric Cancer Patients After Total Gastrectomy: A Prospective Randomized Control Trial (DOPGT_2015)

This is a prospective randomized controlled clinical trial to clarify the effect of early oral nutrition introduction after total gastrectomy in gastric cancer patients on the length of hospital stay, comparing an experimental group vs control group.

Study Overview

Detailed Description

The total gastrectomy is a high complexity surgery that involves a high morbid-mortality. In our center, the postoperative management consisted in 1 week period of non oral intake and total parenteral nutrition. At the 7 day, an oral contrast image is performed to prove the correct function of the anastomosis, in witch case, a progressive oral diet is begin.

In the late 90s, the Fast-track concept (or multimodal perioperative patient care) was introduced in the surgical patients attempting to improve their postoperative course. This new concept includes the preoperative advices related to the surgery, the intensive mobilization after surgery, the early oral diet, and to avoid the routinary use of the nasogastric tube. Some groups have been trying to apply this Fast-track program sporadically in patients submitted to an elective total gastrectomy for gastric cancer, even do, there is still no good evidence to sport these practice.

Based on the reasons exposed before, the investigators design a prospective randomized controlled trial in gastric cancer patients underwent on a total gastrectomy comparing two groups. 24 hours after gastrectomy the investigators will administer oral methylene blue and if no evidence of drainage leakage the participants will be randomized into two groups: one of them with our classical postoperative management, and the other one implements an early oral nutrition protocol, having in considerations its effectiveness, security, and impact on the hospital stay.

Study Type

Interventional

Enrollment (Anticipated)

84

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Barcelona
      • L'Hospitalet de Llobregat, Barcelona, Spain, 08026

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • All patients requiring radical total gastrectomy for gastric cancer.
  • 18 or above years old.
  • Acceptance and signing the full informed consent.

Exclusion Criteria:

  • Patient with poorly controlled diabetes mellitus (glycosylated hemoglobin levels greater than 7%)
  • Emergency surgery.
  • Total gastrectomy with esophagus-jejunal manual suture.
  • Early dehiscence of esophagus-jejunal anastomosis (first 24 hours).
  • Reintervention for abdominal complication in the first 24 hours.
  • Surgery involving large intestinal or colon resections.
  • Proximal resection margin affected requiring a esophagectomy and reconstruction with coloplasty.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: OTHER
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Early oral nutrition
An early oral nutrition with supplements and increased progressively according to an established schedule, start 48 hours after total gastrectomy.
An early oral nutrition with supplements and increased progressively according to an established schedule, start 48 hours after total gastrectomy.
NO_INTERVENTION: control group
In our center, the classical postoperative management consisted in one week period of non oral intake and total parenteral nutrition. At the 7 day, an oral contrast image is performed to prove the correct function of the anastomosis, in witch case, a three days progressive oral diet is begin.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hospital stay
Time Frame: postoperative 1 day to discharge, up to 1 month after surgery
Postoperatory hospital stay in days
postoperative 1 day to discharge, up to 1 month after surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mortality
Time Frame: During the admission, two weeks and one month after surgery
Postoperative Mortality: Deaths occurring during admission and / or within 30 days after surgery or during surgical admission if it lasts longer than 30 days.
During the admission, two weeks and one month after surgery
Hospital readmissions
Time Frame: Two weeks and one month after surgery
It will be considered the income produced within 30 days after the surgical intervention in which the cause of the admission is attributed to a complication in relation to the surgical intervention.
Two weeks and one month after surgery
Weight
Time Frame: First day of hospital admission, two weeks and one month after surgery
weight shall be measured in kilograms
First day of hospital admission, two weeks and one month after surgery
Anastomotic dehiscence
Time Frame: postoperative 1 day to discharge, up to 1 month after surgery

Anastomotic dehiscence: If the intra-abdominal drainage presents a purulent appearance or an amylase determination> 30, suspicion of anastomosis dehiscence will be made; In this situation, a clinical test (intake of methylene blue) radiological test (with oral contrast) or endoscopy will be requested to confirm the diagnosis. Anastomosis dehiscence will be confirmed if any of the following occurs:

  • Exit of methylene blue through intra-abdominal drainage
  • Contrast leakage in a radiological test performed for sepsis
  • Evidence of dehiscence in a fibrogastroscopy
  • Evidence of anastomotic dehiscence during a reintervention
postoperative 1 day to discharge, up to 1 month after surgery
Duodenal stump leak
Time Frame: postoperative 1 day to discharge, up to 1 month after surgery
Intra-abdominal drainage presents a purulent appearance with amylase determination> 30 and a bilirubin value higher than plasmatic bilirubin.
postoperative 1 day to discharge, up to 1 month after surgery
Paralytic ileus
Time Frame: postoperative 1 day to discharge, up to 1 month after surgery

When three of the following criteria are met.

Oral intolerance after the fourth postoperative day Abdominal distention and tympanism No bowel motions or flatus Compatible abdominal x-ray

postoperative 1 day to discharge, up to 1 month after surgery
Intra-Abdominal abscesses
Time Frame: postoperative 1 day to discharge, up to 1 month after surgery
  1. Radiological criteria:

    Air inside the collection Collection with heterogeneous and irregular pickup or wall pickup Collection with heterogeneous content

  2. Isolation of one or more microorganisms in culture after percutaneous collection
postoperative 1 day to discharge, up to 1 month after surgery
Postoperative Hemoperitoneum
Time Frame: postoperative 1 day to discharge, up to 1 month after surgery
Presence of blood in the abdominal cavity after gastrectomy that needs any kind of treatments
postoperative 1 day to discharge, up to 1 month after surgery
Evisceration
Time Frame: postoperative 1 day to discharge, up to 1 month after surgery
Extrusion of viscera outside the body through a surgical incision
postoperative 1 day to discharge, up to 1 month after surgery
Superficial Incisional Surgical Site Infection
Time Frame: postoperative 1 day to discharge, up to 1 month after surgery

Superficial Incisional Surgical Site Infection

Infection within 30 days after the operation and only involves skin and subcutaneous tissue of the incision and at least one of the following:

Purulent drainage with or without laboratory confirmation, from the superficial incision.

Organisms isolated from an aseptically obtained culture of fluid or tissue from the superficial incision.

At least one of the following signs or symptoms of infection: pain or tenderness, localised swelling, redness, or heat and superficial incision is deliberately opened by surgeon, unless incision is culture-negative.

Diagnosis of superficial incisional surgical site infection made by a surgeon or attending physician.

postoperative 1 day to discharge, up to 1 month after surgery
Height
Time Frame: First day of hospital admission, two weeks and one month after surgery
Height shall be measured in meters
First day of hospital admission, two weeks and one month after surgery
Percentage of weight lost
Time Frame: First day of hospital admission, two weeks and one month after surgery
Percentage of weight lost shall be measured in percentage
First day of hospital admission, two weeks and one month after surgery
Impedancemetry
Time Frame: First day of hospital admission, two weeks and one month after surgery

The impedanciometry will record:

Phase-angle Na / K ratio Basal metabolism (Kcal) Fat mass percentage Muscle mass percentage Cell mass percentage Extracellular mass percentage

First day of hospital admission, two weeks and one month after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Leandre Farran Teixidor, PhD, MD, Bellvitge University Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

October 20, 2017

Primary Completion (ANTICIPATED)

October 1, 2022

Study Completion (ANTICIPATED)

September 1, 2023

Study Registration Dates

First Submitted

July 7, 2017

First Submitted That Met QC Criteria

August 21, 2017

First Posted (ACTUAL)

August 22, 2017

Study Record Updates

Last Update Posted (ACTUAL)

February 17, 2021

Last Update Submitted That Met QC Criteria

February 16, 2021

Last Verified

February 1, 2021

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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