GRO-HD: Glycaemic Response to Oral Nutrition Support During Haemodialysis

Sponsor
King's College Hospital NHS Trust (Other)
Overall Status
Completed
CT.gov ID
NCT02989688
Collaborator
King's College London (Other)
24
1
3
23
1

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Nepro HP (Abbott Nutrition)
  • Dietary Supplement: Fortisip compact protein 125 ml + Calogen 20ml (Nutricia)
  • Dietary Supplement: Fortisip compact 125 ml (Nutricia)
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
24 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Glycaemic Response to Oral Nutrition Support During Haemodialysis
Study Start Date :
Jan 1, 2015
Actual Primary Completion Date :
Dec 1, 2016
Actual Study Completion Date :
Dec 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: modified carbohydrate drink

Dietary Supplement - renal specific slow release carbohydrate ONS (220 ml Nepro HP (Abbott Nutrition)

Dietary Supplement: Nepro HP (Abbott Nutrition)
oral nutritional supplement drink with modified carbohydrate composition

Active Comparator: macronutrient matched drink

Dietary Supplement - 125 ml Fortisip Compact Protein (Nutricia) plus 20ml Calogen (Nutricia)

Dietary Supplement: Fortisip compact protein 125 ml + Calogen 20ml (Nutricia)
Fortisip compact protein 125 ml + Calogen 20ml (Nutricia) oral nutritional supplement drink macronutrient matched with standard carbohydrate composition

Active Comparator: standard drink

Dietary Supplement - 125 ml Fortisip compact (Nutricia)

Dietary Supplement: Fortisip compact 125 ml (Nutricia)
Fortisip compact 125 ml (Nutricia) oral nutritional supplement drink - standard

Outcome Measures

Primary Outcome Measures

  1. Blood glucose response curve [3 hour]

    Mean incremental area under the curve for blood glucose response to intervention over 3 hours

Secondary Outcome Measures

  1. Peak blood glucose reading within 3 hours [3 hours]

  2. Appetite score pre and post ONS [3 hours]

    likert scale

  3. Flavour acceptability scale for ONS product [3 hours]

    likert scale

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 King's College Hospital London United Kingdom SE5 9RS

Sponsors and Collaborators

  • King's College Hospital NHS Trust
  • King's College London

Investigators

  • Principal Investigator: Helen L MacLaughlin, PhD, Clinical Lecturer

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
King's College Hospital NHS Trust
ClinicalTrials.gov Identifier:
NCT02989688
Other Study ID Numbers:
  • KingCHL
First Posted:
Dec 12, 2016
Last Update Posted:
Dec 12, 2016
Last Verified:
Jan 1, 2016
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 12, 2016