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Feasibility Study Comparing Enteral vs Parenteral Nutritional Outcomes in Autologous Stem Cell Transplant Patients

Primary Purpose

Malignant Hematologic Neoplasm

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Parenteral Nutrition/Enteral Nutrition
Sponsored by
Lawson Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malignant Hematologic Neoplasm focused on measuring Non- Hodgkin's Lymphoma, Hodgkin's Lymphoma, Multiple Myeloma, AHSCT

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All adult patients aged 18 to 75 years.
  • Patients admitted to Victoria Hospital undergoing AHSCT on C7 unit.
  • Patient consented to participate in the study
  • Patients diagnosed with the following conditions: Non- Hodgkin's Lymphoma (all types), Hodgkin's Lymphoma (all subtypes) and Multiple Myeloma
  • Patients receiving any of the following: Conditioning chemotherapy: Melphalan, Etoposide/Melphalan, or Carmustine, Etoposide, Cytarabine, Melphalan
  • Have a functional Gastrointestinal tract

Exclusion Criteria:

  • Intestinal obstruction
  • Patients with nasal deformities, tumors of nasal tracts or upper nare obstruction.
  • Patients with active bacteremia while proceeding with transplant
  • Patients with active malignancy of Upper GI tract, not in remission as evidenced by recent imaging studies (< 4 weeks)
  • Patients with any GI bleeding, paralytic ileus, obstruction, or any other GI condition which excludes use of the GI system for nutritional support as these patients will require PN feeding only and cannot be randomized

Sites / Locations

  • London Health Sciences Centre-Victoria HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Parenteral Nutrition

Enteral Nutrition

Arm Description

Patients who have been randomized to receive PN will be started on day 5 post AHSCT. This will be if patient intake is < 80% of usual oral intake at that time. The central venous catheter required for PN administration will be already in place for AHSCT treatment, prior to admission and pre-transplant evaluation. Nutritional support will continue until oral intake is >50% or until the patient is ready for discharge if intake remains < 50% of recommendations.

Patients who have been randomized to receive EN will have a Nasogastric tube (NGT) inserted on day 5 post AHSCT, prior to start of Enteral feeds. This would be a polyurethane tube, 8-10 French, which will be inserted by physician or Nurse Practitioner with position confirmed by radiological examination. This will be if patient intake is < 80% of usual oral intake at that time. Nutritional support will continue until oral intake is >50% or until the patient is ready for discharge if intake remains < 50% of recommendations.

Outcomes

Primary Outcome Measures

Enrollment of patients
The number of patients enrolled

Secondary Outcome Measures

quadriceps muscle layer thickness
Maintenance and/or improvement of quadriceps muscle layer thickness (QMLT) measurement: measured by ultrasound.
Duration of Support
A comparison of duration in days a patient will require enteral or parenteral nutritional support during their admission.
Changes in costs
The cost of daily total PN is $80/day and cost of EN feeds would be $40/day. This is a 50% change in costs.
Hospital Stay
Length of hospital stay (decrease by 1+/-2 days)
Mortality
Mortality on Day+30 Post AHSCT
Changes in body fat
Measuring the changes in percentage of body fat mass using Bioelectric Impedance Analysis
Changes in Lean Muscle
Measuring the changes in percentage lean muscle mass using Bioelectric Impedance Analysis
Changes in costs to hospital when using enteral nutritional
the measurement the length of their stay in the hospital by days, fewer days of hospitalization = lower costs and more days of hospitalization = greater costs
Transition from EN to oral feeding
Successful transition from EN to oral feeding versus Parenteral Nutrition to oral feeding defined by 50% oral intake on Day+15 of AHSCT.

Full Information

First Posted
April 24, 2019
Last Updated
March 27, 2020
Sponsor
Lawson Health Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT04024618
Brief Title
Feasibility Study Comparing Enteral vs Parenteral Nutritional Outcomes in Autologous Stem Cell Transplant Patients
Official Title
A Pilot Feasibility Study of Nutritional Outcomes in Autologous Hematopoietic Stem Cell Transplant Recipients Comparing Enteral Nutrition Versus Parenteral Nutrition
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 20, 2019 (Actual)
Primary Completion Date
August 30, 2020 (Anticipated)
Study Completion Date
December 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lawson Health Research Institute

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
This study will highlight that Enteral Nutrition (EN) is as effective in nutritionally supporting as Parenteral Nutrition (PN) in this group of patients undergoing an autologous hematopoietic stem cell transplantation (AHSCT). The rationale of this study is to compare nutritional, medical, cost and Quality of Life (QOL) outcomes in patients receiving either EN or PN nutritional support in patients. The main outcomes are to examine are nutritional status, medical complications, cost and QOL before and after AHSCT.
Detailed Description
This will be a pilot open randomized study. The study will be conducted at the inpatient setting at London Health Sciences Centre in London, ON. Forty patients will be randomized in permutated blocks independently by Statistician, to either the EN or PN group on admission to the unit. The baseline evaluations are blood work, Bioelectric Impedance Analysis (BIA), Subjective Global Assessment (SGA), Body Mass Index (BMI) calculation, ultrasound, and a medical evaluation. Patients do have the right to refuse either or both types of nutritional support. As part of standard care, the risks and benefits of nutritional support for both EN and PN will be explained to the patient. Consent will be obtained prior to admission. Most of these patients initially continue to maintain their oral intake even after chemotherapy. On Day 5+/- 1 day after transplantation, the randomized nutrition therapy will only be initiated only if patient intake is < 80% of usual intake, where they will be provided with 25-35 kcal/kg/day, 1.2-1.5g of protein/kg/day, and omega-3 to supplement any oral intake the patient might not have. If the intake is >80% of required intake, initiation of randomized therapy will only happen on the day the intake falls to <80% of required nutritional intake. Patients will be monitored until Day 15 where post-transplant evaluations will be conducted: blood work, BIA, SGA, ultrasound, BMI, food records, and medical evaluation. If at that time, patients are not consuming 50% of energy from oral feeds, nutrition therapy will continue until oral goal is met or until discharge for medical reasons. Patients will be assessed at Day+30 post-transplant in clinic and the following will be completed blood work, BIA, SGA, BMI, food records, ultrasound, medical complications and a QOL assessment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Hematologic Neoplasm
Keywords
Non- Hodgkin's Lymphoma, Hodgkin's Lymphoma, Multiple Myeloma, AHSCT

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomization will be 1:1, both EN and PN arms. The patients will be randomized in permutated blocks independently by Statistician.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Parenteral Nutrition
Arm Type
Active Comparator
Arm Description
Patients who have been randomized to receive PN will be started on day 5 post AHSCT. This will be if patient intake is < 80% of usual oral intake at that time. The central venous catheter required for PN administration will be already in place for AHSCT treatment, prior to admission and pre-transplant evaluation. Nutritional support will continue until oral intake is >50% or until the patient is ready for discharge if intake remains < 50% of recommendations.
Arm Title
Enteral Nutrition
Arm Type
Experimental
Arm Description
Patients who have been randomized to receive EN will have a Nasogastric tube (NGT) inserted on day 5 post AHSCT, prior to start of Enteral feeds. This would be a polyurethane tube, 8-10 French, which will be inserted by physician or Nurse Practitioner with position confirmed by radiological examination. This will be if patient intake is < 80% of usual oral intake at that time. Nutritional support will continue until oral intake is >50% or until the patient is ready for discharge if intake remains < 50% of recommendations.
Intervention Type
Procedure
Intervention Name(s)
Parenteral Nutrition/Enteral Nutrition
Intervention Description
Patients randomized to the parenteral nutrition arm will receive nutrition by IV and patients randomized to the enteral nutrition arm will receive nutrition by NG tube.
Primary Outcome Measure Information:
Title
Enrollment of patients
Description
The number of patients enrolled
Time Frame
30 days
Secondary Outcome Measure Information:
Title
quadriceps muscle layer thickness
Description
Maintenance and/or improvement of quadriceps muscle layer thickness (QMLT) measurement: measured by ultrasound.
Time Frame
21 days
Title
Duration of Support
Description
A comparison of duration in days a patient will require enteral or parenteral nutritional support during their admission.
Time Frame
21 days
Title
Changes in costs
Description
The cost of daily total PN is $80/day and cost of EN feeds would be $40/day. This is a 50% change in costs.
Time Frame
21 days
Title
Hospital Stay
Description
Length of hospital stay (decrease by 1+/-2 days)
Time Frame
21 days
Title
Mortality
Description
Mortality on Day+30 Post AHSCT
Time Frame
30 days
Title
Changes in body fat
Description
Measuring the changes in percentage of body fat mass using Bioelectric Impedance Analysis
Time Frame
21 Days
Title
Changes in Lean Muscle
Description
Measuring the changes in percentage lean muscle mass using Bioelectric Impedance Analysis
Time Frame
21 Days
Title
Changes in costs to hospital when using enteral nutritional
Description
the measurement the length of their stay in the hospital by days, fewer days of hospitalization = lower costs and more days of hospitalization = greater costs
Time Frame
21 Days
Title
Transition from EN to oral feeding
Description
Successful transition from EN to oral feeding versus Parenteral Nutrition to oral feeding defined by 50% oral intake on Day+15 of AHSCT.
Time Frame
15 Days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All adult patients aged 18 to 75 years. Patients admitted to Victoria Hospital undergoing AHSCT on C7 unit. Patient consented to participate in the study Patients diagnosed with the following conditions: Non- Hodgkin's Lymphoma (all types), Hodgkin's Lymphoma (all subtypes) and Multiple Myeloma Patients receiving any of the following: Conditioning chemotherapy: Melphalan, Etoposide/Melphalan, or Carmustine, Etoposide, Cytarabine, Melphalan Have a functional Gastrointestinal tract Exclusion Criteria: Intestinal obstruction Patients with nasal deformities, tumors of nasal tracts or upper nare obstruction. Patients with active bacteremia while proceeding with transplant Patients with active malignancy of Upper GI tract, not in remission as evidenced by recent imaging studies (< 4 weeks) Patients with any GI bleeding, paralytic ileus, obstruction, or any other GI condition which excludes use of the GI system for nutritional support as these patients will require PN feeding only and cannot be randomized
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Uday Deotare, MD
Phone
519-685-8500
Ext
58479
Email
Uday.Deotare@lhsc.on.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Maisam Abouzeenni, BHS
Phone
519-685-8500
Ext
56840
Email
Maisam.Abouzeenni@lhsc.on.ca
Facility Information:
Facility Name
London Health Sciences Centre-Victoria Hospital
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5W9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Uday Deotare, MD
Phone
519-685-8500
Ext
76616
Email
Uday.Deotare@lhsc.on.ca

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The investigators do not plan on sharing individual participant data to other researchers
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Feasibility Study Comparing Enteral vs Parenteral Nutritional Outcomes in Autologous Stem Cell Transplant Patients

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