Trial on Impact on the Hospital Stay, of an Early Oral Nutrition Protocol Applied to Patients After Total Gastrectomy. (DOPGT_2015)
Primary Purpose
Early Oral Nutrition After Total Gastrectomy, Gastric Cancer
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Early oral nutrition
Sponsored by
About this trial
This is an interventional other trial for Early Oral Nutrition After Total Gastrectomy
Eligibility Criteria
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.
Sites / Locations
- Leandre Farran TeixidorRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Early oral nutrition
control group
Arm Description
An early oral nutrition with supplements and increased progressively according to an established schedule, start 48 hours after total gastrectomy.
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.
Outcomes
Primary Outcome Measures
Hospital stay
Postoperatory hospital stay in days
Secondary Outcome Measures
Mortality
Postoperative Mortality: Deaths occurring during admission and / or within 30 days after surgery or during surgical admission if it lasts longer than 30 days.
Hospital readmissions
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.
Weight
weight shall be measured in kilograms
Anastomotic dehiscence
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
Duodenal stump leak
Intra-abdominal drainage presents a purulent appearance with amylase determination> 30 and a bilirubin value higher than plasmatic bilirubin.
Paralytic ileus
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
Intra-Abdominal abscesses
Radiological criteria:
Air inside the collection Collection with heterogeneous and irregular pickup or wall pickup Collection with heterogeneous content
Isolation of one or more microorganisms in culture after percutaneous collection
Postoperative Hemoperitoneum
Presence of blood in the abdominal cavity after gastrectomy that needs any kind of treatments
Evisceration
Extrusion of viscera outside the body through a surgical incision
Superficial Incisional Surgical Site Infection
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.
Height
Height shall be measured in meters
Percentage of weight lost
Percentage of weight lost shall be measured in percentage
Impedancemetry
The impedanciometry will record:
Phase-angle Na / K ratio Basal metabolism (Kcal) Fat mass percentage Muscle mass percentage Cell mass percentage Extracellular mass percentage
Full Information
NCT ID
NCT03257280
First Posted
July 7, 2017
Last Updated
February 16, 2021
Sponsor
Hospital Universitari de Bellvitge
1. Study Identification
Unique Protocol Identification Number
NCT03257280
Brief Title
Trial on Impact on the Hospital Stay, of an Early Oral Nutrition Protocol Applied to Patients After Total Gastrectomy. (DOPGT_2015)
Official Title
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)
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 20, 2017 (Actual)
Primary Completion Date
October 2022 (Anticipated)
Study Completion Date
September 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitari de Bellvitge
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Early Oral Nutrition After Total Gastrectomy, Gastric Cancer
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
84 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Early oral nutrition
Arm Type
Experimental
Arm Description
An early oral nutrition with supplements and increased progressively according to an established schedule, start 48 hours after total gastrectomy.
Arm Title
control group
Arm Type
No Intervention
Arm Description
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.
Intervention Type
Other
Intervention Name(s)
Early oral nutrition
Intervention Description
An early oral nutrition with supplements and increased progressively according to an established schedule, start 48 hours after total gastrectomy.
Primary Outcome Measure Information:
Title
Hospital stay
Description
Postoperatory hospital stay in days
Time Frame
postoperative 1 day to discharge, up to 1 month after surgery
Secondary Outcome Measure Information:
Title
Mortality
Description
Postoperative Mortality: Deaths occurring during admission and / or within 30 days after surgery or during surgical admission if it lasts longer than 30 days.
Time Frame
During the admission, two weeks and one month after surgery
Title
Hospital readmissions
Description
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.
Time Frame
Two weeks and one month after surgery
Title
Weight
Description
weight shall be measured in kilograms
Time Frame
First day of hospital admission, two weeks and one month after surgery
Title
Anastomotic dehiscence
Description
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
Time Frame
postoperative 1 day to discharge, up to 1 month after surgery
Title
Duodenal stump leak
Description
Intra-abdominal drainage presents a purulent appearance with amylase determination> 30 and a bilirubin value higher than plasmatic bilirubin.
Time Frame
postoperative 1 day to discharge, up to 1 month after surgery
Title
Paralytic ileus
Description
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
Time Frame
postoperative 1 day to discharge, up to 1 month after surgery
Title
Intra-Abdominal abscesses
Description
Radiological criteria:
Air inside the collection Collection with heterogeneous and irregular pickup or wall pickup Collection with heterogeneous content
Isolation of one or more microorganisms in culture after percutaneous collection
Time Frame
postoperative 1 day to discharge, up to 1 month after surgery
Title
Postoperative Hemoperitoneum
Description
Presence of blood in the abdominal cavity after gastrectomy that needs any kind of treatments
Time Frame
postoperative 1 day to discharge, up to 1 month after surgery
Title
Evisceration
Description
Extrusion of viscera outside the body through a surgical incision
Time Frame
postoperative 1 day to discharge, up to 1 month after surgery
Title
Superficial Incisional Surgical Site Infection
Description
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.
Time Frame
postoperative 1 day to discharge, up to 1 month after surgery
Title
Height
Description
Height shall be measured in meters
Time Frame
First day of hospital admission, two weeks and one month after surgery
Title
Percentage of weight lost
Description
Percentage of weight lost shall be measured in percentage
Time Frame
First day of hospital admission, two weeks and one month after surgery
Title
Impedancemetry
Description
The impedanciometry will record:
Phase-angle Na / K ratio Basal metabolism (Kcal) Fat mass percentage Muscle mass percentage Cell mass percentage Extracellular mass percentage
Time Frame
First day of hospital admission, two weeks and one month after surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Leandre Farran Teixidor, PhD, MD
Phone
+34-93-335-90-11
Ext
2316
Email
lfarran@bellvitgehospital.cat
First Name & Middle Initial & Last Name or Official Title & Degree
Fernando Estremiana Garcia, MD
Phone
+34-93-335-90-11
Ext
2316
Email
festremiana@bellvitgehospital.cat
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leandre Farran Teixidor, PhD, MD
Organizational Affiliation
Bellvitge University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Leandre Farran Teixidor
City
L'Hospitalet de Llobregat
State/Province
Barcelona
ZIP/Postal Code
08026
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Leandre Farran Teixidor, PhD, MD
Phone
+34-93-335-90-11
Ext
2316
Email
lfarran@bellvitgehospital.cat
First Name & Middle Initial & Last Name & Degree
Fernando Estremiana Garcia, MD
Phone
+34-93-335-90-11
Ext
2316
Email
festremiana@bellvitgehospital.cat
12. IPD Sharing Statement
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Trial on Impact on the Hospital Stay, of an Early Oral Nutrition Protocol Applied to Patients After Total Gastrectomy. (DOPGT_2015)
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