Glycaemic Response to Oral Nutrition Support During Haemodialysis (GRO-HD)
Primary Purpose
Diabetes, Chronic Kidney Disease, End Stage Renal Failure on Dialysis
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Nepro HP (Abbott Nutrition)
Fortisip compact protein 125 ml + Calogen 20ml (Nutricia)
Fortisip compact 125 ml (Nutricia)
Sponsored by
About this trial
This is an interventional treatment trial for Diabetes
Eligibility Criteria
Inclusion Criteria:
- Type 1 or type 2 diabetes
- End stage kidney disease on haemodialysis
- Body mass index 18.5-35kg/m2
- Able to provide written informed consent
Exclusion Criteria:
• Infection or course of antibiotics in the last month
Sites / Locations
- King's College Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
modified carbohydrate drink
macronutrient matched drink
standard drink
Arm Description
Dietary Supplement - renal specific slow release carbohydrate ONS (220 ml Nepro HP (Abbott Nutrition)
Dietary Supplement - 125 ml Fortisip Compact Protein (Nutricia) plus 20ml Calogen (Nutricia)
Dietary Supplement - 125 ml Fortisip compact (Nutricia)
Outcomes
Primary Outcome Measures
Blood glucose response curve
Mean incremental area under the curve for blood glucose response to intervention over 3 hours
Secondary Outcome Measures
Peak blood glucose reading within 3 hours
Appetite score pre and post ONS
likert scale
Flavour acceptability scale for ONS product
likert scale
Full Information
NCT ID
NCT02989688
First Posted
January 20, 2016
Last Updated
December 7, 2016
Sponsor
King's College Hospital NHS Trust
Collaborators
King's College London
1. Study Identification
Unique Protocol Identification Number
NCT02989688
Brief Title
Glycaemic Response to Oral Nutrition Support During Haemodialysis
Acronym
GRO-HD
Official Title
Glycaemic Response to Oral Nutrition Support During Haemodialysis
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
December 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
King's College Hospital NHS Trust
Collaborators
King's College London
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients with kidney, or renal, failure require life-saving treatment with regular dialysis. Dialysis is a form of treatment that simulates some kidney functions; to remove harmful waste products and extra water from the blood. Almost one-third of people with kidney failure also have diabetes, as diabetes is one of the leading causes of kidney disease in the United Kingdom, usually due to poor blood sugar control over a long period of time. Malnutrition is common in patients needing dialysis due to kidney failure causing fatigue, taste changes and a build up of waste products, which can reduce appetite. Treatment of malnutrition involves increasing both the energy and protein intake from food and drinks, and milk-drink style specialist nutrition drinks are often given to dialysis patients due to their specific dietary needs. These nutrition drinks can increase blood sugar levels and optimal control for diabetes may be difficult. This research study aims to measure the blood sugar response to a "slow-release" sugar nutrition drink specifically designed for dialysis patients, which may result in a lower blood sugar level, compared to standard nutrition drinks, consumed during a dialysis session. 28 patients with diabetes and having regular dialysis treatment will enrol in the study. Patients will be asked to drink 1 of 3 different nutrition drinks, once a week for 3 weeks during their regular dialysis treatment. Blood sugar levels will be measured from the blood samples taken from the patient's circulation directly before it enters the dialysis machine over 3 hours and the maximum blood sugar reading and total blood sugar response will be measured. Differences between the 3 drinks will be tested statistically. The results will help to advise patients with diabetes and kidney failure on the most suitable type of nutrition drink to consume during dialysis.
Detailed Description
Patients with end stage kidney disease requiring dialysis are at the highest risk for cardiovascular disease, and many of our dialysis population also have diabetes. Malnutrition is common in patients undergoing dialysis and causes are multifactorial. Oral nutrition support is the first line treatment for malnutrition, and often includes the use of liquid nutrition supplements, especially in dialysis patients due to the already restricted diet required to maintain electrolyte balance. Oral nutrition supplements (ONS) can raise serum blood glucose levels and optimal control for diabetes may be difficult when ONS are required. This study aims to evaluate the post-prandial response to a newly re-formulated slow release carbohydrate renal specific oral nutrition supplement, compared to standard and macro-nutrient matched ONS products, during haemodialysis, using a randomised cross-over trial design. 28 patients with diabetes and end stage kidney disease undergoing haemodialysis will be recruited to the study, including 8 in the pilot phase and 20 in the study. Patients will be randomised in a crossover design to 3 study treatments over 3 weeks - slow release CHO ONS, macronutrient matched ONS, and standard ONS. Central blood glucose levels will be measured over 3 hours and the peak and mean incremental area under the curve (iAUC) of the post prandial blood glucose response will be calculated for each study treatment. Differences between treatments will be determined with repeated measures analysis of co-variance (ANCOVA). The acute effect of different nutritional supplements on blood glucose will be discussed in the context of maintaining optimal blood glucose control during dialysis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Chronic Kidney Disease, End Stage Renal Failure on Dialysis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
modified carbohydrate drink
Arm Type
Active Comparator
Arm Description
Dietary Supplement - renal specific slow release carbohydrate ONS (220 ml Nepro HP (Abbott Nutrition)
Arm Title
macronutrient matched drink
Arm Type
Active Comparator
Arm Description
Dietary Supplement - 125 ml Fortisip Compact Protein (Nutricia) plus 20ml Calogen (Nutricia)
Arm Title
standard drink
Arm Type
Active Comparator
Arm Description
Dietary Supplement - 125 ml Fortisip compact (Nutricia)
Intervention Type
Dietary Supplement
Intervention Name(s)
Nepro HP (Abbott Nutrition)
Intervention Description
oral nutritional supplement drink with modified carbohydrate composition
Intervention Type
Dietary Supplement
Intervention Name(s)
Fortisip compact protein 125 ml + Calogen 20ml (Nutricia)
Intervention Description
Fortisip compact protein 125 ml + Calogen 20ml (Nutricia) oral nutritional supplement drink macronutrient matched with standard carbohydrate composition
Intervention Type
Dietary Supplement
Intervention Name(s)
Fortisip compact 125 ml (Nutricia)
Intervention Description
Fortisip compact 125 ml (Nutricia) oral nutritional supplement drink - standard
Primary Outcome Measure Information:
Title
Blood glucose response curve
Description
Mean incremental area under the curve for blood glucose response to intervention over 3 hours
Time Frame
3 hour
Secondary Outcome Measure Information:
Title
Peak blood glucose reading within 3 hours
Time Frame
3 hours
Title
Appetite score pre and post ONS
Description
likert scale
Time Frame
3 hours
Title
Flavour acceptability scale for ONS product
Description
likert scale
Time Frame
3 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Type 1 or type 2 diabetes
End stage kidney disease on haemodialysis
Body mass index 18.5-35kg/m2
Able to provide written informed consent
Exclusion Criteria:
• Infection or course of antibiotics in the last month
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Helen L MacLaughlin, PhD
Organizational Affiliation
Clinical Lecturer
Official's Role
Principal Investigator
Facility Information:
Facility Name
King's College Hospital
City
London
ZIP/Postal Code
SE5 9RS
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32390133
Citation
Mah JY, Choy SW, Roberts MA, Desai AM, Corken M, Gwini SM, McMahon LP. Oral protein-based supplements versus placebo or no treatment for people with chronic kidney disease requiring dialysis. Cochrane Database Syst Rev. 2020 May 11;5(5):CD012616. doi: 10.1002/14651858.CD012616.pub2.
Results Reference
derived
Learn more about this trial
Glycaemic Response to Oral Nutrition Support During Haemodialysis
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