Impact of Various Diets on Surgical Complications (IMM4)
Primary Purpose
Complication,Postoperative
Status
Unknown status
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Immunonutrition
High-protein
Standard ONS
Sponsored by
About this trial
This is an interventional treatment trial for Complication,Postoperative
Eligibility Criteria
Inclusion Criteria:
- no sign of malnutrition (defined as one of the following unintentional weight loss by at least 10% or body mass index (BMI) < 18),
- good general status (Karnofsky Performance Index > 80,
- Eastern Cooperative Oncology Group (ECOG) grade 0 or 1);
- no confirmed neoplastic dissemination no severe concomitant disease (heart, lung, kidney, liver failure, chronic obstructive pulmonary disease [COPD], coronary aortic bypass graft [CABG], etc.),
- no history of known allergies or drug intolerance to analyzed substances.
Exclusion Criteria:
- Patients malnourished or with metastatic disease,
- pregnant,
- in poor general status (Karnofsky <80, Eastern Cooperative Oncology Group (ECOG) > 1),
- recent history of severe heart, lung, kidney or liver failure,
- history of allergies or drug intolerance
Sites / Locations
- Narodowy Instytut OnkologiiRecruiting
- Stanley Dudrick's Memorial HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Active Comparator
Arm Label
Immunonutrition
High-protein diet
Standard nutrition
Arm Description
Oral immunonutrition containing arginine, omega-PUFAs and antioxidants
Oral nutrition with high-protein content
Oral nutrition with standard components
Outcomes
Primary Outcome Measures
Surgical complications
Number and type of surgical complications
Infectious complications
Number and type of infectious complications
Secondary Outcome Measures
Length of stay
Days of hospital stay after the operation
Full Information
NCT ID
NCT05069402
First Posted
September 25, 2021
Last Updated
October 6, 2021
Sponsor
Stanley Dudrick's Memorial Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05069402
Brief Title
Impact of Various Diets on Surgical Complications
Acronym
IMM4
Official Title
Impact of Immunomodulating Oral Nutrition on Surgical Complications
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
January 31, 2023 (Anticipated)
Study Completion Date
March 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanley Dudrick's Memorial Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The optimalisation of the health status of patients scheduled for major surgery has been considered to be the most important point of perioperative care, and nutritional intervention has been perceived a key point of that intervention. Immunomodulating diets were thought to reduce cmplications, hoever recent studies put that opnion in doubt. This study was designed to assess the actual clinical significance of oral immunonutrition.
Detailed Description
The optimalisation of the health status of patients scheduled for major surgery has been considered to be the most important point of perioperative care, and nutritional intervention has been perceived a key point of that intervention. Italian studies followed by metanalyses demonstrated the superiority of immunomodulating diets (IM) over any other preoperative nutrition, hence the surgical guidelines for enteral nutrition published by European Society for Clinical Nutrition and Metabolism (ESPEN) in 2006 recommended to use IM for 7-14 days preoperatively in all patients undergoing major surgeries. Some authors questioned IM by showing no benefit of IM over standard enteral nutrition. Other authors observed similar results.The debate was far from being over - in 2015 a new metanalysis stated that perioperative enteral nutrition is the best option for managing clinical status of patients who underwent selective surgery for gastrointestinal cancer. One year later, ESPEN changed its surgical recommendations and advised to use IM preoperatively in malnourished and perioperatively in well-nourished patients. American recommendations remained unchanged and, according to them, it is advised to use IM preoperatively in all surgical patients, however, high-protein nutrition could also be an beneficial option.
To address those doubts and to assess the actual clinical significance of oral immunonutrition, a randomized, two center, prospective clinical trial was conducted.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Complication,Postoperative
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomisation into 3 arms
Masking
Care ProviderInvestigatorOutcomes Assessor
Masking Description
The physician is unaware of the type of the intervention. The type of intervention is given by the independent person to dietitian instructing the patient how to use the product.
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Immunonutrition
Arm Type
Experimental
Arm Description
Oral immunonutrition containing arginine, omega-PUFAs and antioxidants
Arm Title
High-protein diet
Arm Type
Active Comparator
Arm Description
Oral nutrition with high-protein content
Arm Title
Standard nutrition
Arm Type
Active Comparator
Arm Description
Oral nutrition with standard components
Intervention Type
Dietary Supplement
Intervention Name(s)
Immunonutrition
Intervention Description
diet with immunonutrients
Intervention Type
Dietary Supplement
Intervention Name(s)
High-protein
Intervention Description
Oral nutrition with high-protein content
Intervention Type
Dietary Supplement
Intervention Name(s)
Standard ONS
Intervention Description
Oral nutrition with standard ingredients
Primary Outcome Measure Information:
Title
Surgical complications
Description
Number and type of surgical complications
Time Frame
6 months
Title
Infectious complications
Description
Number and type of infectious complications
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Length of stay
Description
Days of hospital stay after the operation
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
no sign of malnutrition (defined as one of the following unintentional weight loss by at least 10% or body mass index (BMI) < 18),
good general status (Karnofsky Performance Index > 80,
Eastern Cooperative Oncology Group (ECOG) grade 0 or 1);
no confirmed neoplastic dissemination no severe concomitant disease (heart, lung, kidney, liver failure, chronic obstructive pulmonary disease [COPD], coronary aortic bypass graft [CABG], etc.),
no history of known allergies or drug intolerance to analyzed substances.
Exclusion Criteria:
Patients malnourished or with metastatic disease,
pregnant,
in poor general status (Karnofsky <80, Eastern Cooperative Oncology Group (ECOG) > 1),
recent history of severe heart, lung, kidney or liver failure,
history of allergies or drug intolerance
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stanislaw Klek, PhD
Phone
+48604293566
Email
klek@poczta.onet.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stanislaw Klek, PhD
Organizational Affiliation
Stanley Dudrick's Memorial Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Narodowy Instytut Onkologii
City
Krakow
State/Province
Malopolska
ZIP/Postal Code
31-115
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stanislaw Klek, PhD
Phone
60293566
Email
stanislaw.klek@onkologia.krakow.pl
Facility Name
Stanley Dudrick's Memorial Hospital
City
Skawina
State/Province
Malopolska
ZIP/Postal Code
32-050
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stanley Dudrick's M Hospital
Phone
604293566
Email
klek@poczta.onet.pl
Ext
Klek
Email
klek@poczta.onet.pl
First Name & Middle Initial & Last Name & Degree
Stanislaw Klek
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Time Frame
12 months
IPD Sharing Access Criteria
any health professional
Learn more about this trial
Impact of Various Diets on Surgical Complications
We'll reach out to this number within 24 hrs