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临床试验/NCT02371694
NCT02371694已完成不适用

What is the Dose Response of Varying Meal Content of Fat on Postprandial Glycaemia in Children With Type 1 Diabetes Mellitus?

Cork University Hospital1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2015年2月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
1
主要终点
Glycaemic excursion

研究概览

简要总结

Background: Based on international evidence, current management of people with T1DM on intensive insulin therapy (IIT) use algorithms based on the meal carbohydrate content (MCC) to calculate the prandial insulin dose. Typically, these calculations do not take into account the protein or fat content of the meal. There is a lack of clinical advice for optimal management of high protein/fat meals due to a paucity of evidence regarding the impact of protein/fat on glycaemic control.

Objective: To determine the mean glucose excursion from fasting (measured by continuous glucose monitoring, CGMS) at each 30 minute interval over the 8 hour postprandial period for each test condition. Protein effects will be looked at in a separate parallel study in Australia.

Hypothesis: The fat content of a meal will cause a dose-response change in the postprandial glucose concentration in children with T1DM.

Research Design and Methods: Randomised cross-over study involving thirty patients. Inclusion criteria: T1DM >1 year, aged 8-18 years, with HbA1c <8% and BMI <91st centile, on intensive insulin therapy. Participants will be given a test meal on 6 consecutive nights in random order; 4 test meals varying in fat content, and one 20g carbohydrate test meal with zero fat given as control meal. A CGMS will be used to assess glucose responses at 5 minute intervals for 8 hours after test meal consumption. The relationship between the fat loads in the test meals and the mean change in postprandial glucose concentration will be analysed and described.

Conclusions: This study will determine whether fat causes dose dependent response in glucose concentrations leading to refining the guidelines and possible adjustment of insulin doses for the fat content of a meal.

详细描述

  1. Aims of the project To determine the postprandial glucose dose-response curves response to varying fat amounts by studying various parameters (glycaemic excursion, rate of glucose level increase, area under the curve, percent time in target glucose range, maximal glucose excursion, time to maximal glucose excursion and time until the glucose level returns to fasting concentration) provided by continuous glucose monitoring over a 6 day study period with a view to provide data to calculate an accurate insulin dosing schedule to account for varying dietary fat ingestion.

Objective 1 To define the impact of varying quantities (dose) of fat on the post-prandial glucose concentrations i.e. determine the relationship between the fat load in the test meals and the mean change in postprandial glucose concentrations.

Objective 2 To compare the impact of the varying fat quantities in the test meals each with a control carbohydrate snack (20g) without extra insulin. 2. Protocol Participants will be contacted daily for one week prior to the study to review their overnight and fasting glucose concentrations and if necessary, adjust their insulin doses. The study will be carried out during a week long period for each patient. Participants will be given test meals over 6 consecutive days in random order, with 5 test meals varying in lipid content and one carbohydrate (20g) test meal as comparator. A continuous glucose monitoring system (CGMS) will be inserted on the day of the first test meal and will be removed at the completion of the sixth night.

To define the impact of lipid on the post-prandial glucose concentration, participants will consume a standardised meal at 18:00hours and receive a standard insulin bolus by injection or pump (using standard wave bolus if on insulin pump) based on the meal carbohydrate content. At 22:00 hours the participants will consume a lipid test meal dose (varying fat content of 2.5, 12.5, 25, 37.5, 50g) or carbohydrate snack 20g. The calculations of the fat doses have been based on the Pankowska algorithm [3] which recommends additional insulin for every 100 kcal fat or protein. There will be randomised order of test meals.

Test meals will be formulated to be palatable, consumed within 5 minutes and to contain negligible carbohydrate, protein and fibre. A dietician will design the test meals in conjunction with the co-investigator in detail to ensure ease of formulation and practical administration.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
8 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with T1DM for more than 1 year
  • HbA1c less than 8%
  • BMI less than 91st centile
  • on intensive insulin therapy

排除标准

  • 未提供

研究组 & 干预措施

Fat Test drink (25g)

Experimental

This drink contains 25g sunflower oil and vehicle (almond milk, chocolate drink powder, sweetener)

干预措施: Test drink (Other)

Fat Test drink (50g)

Experimental

This drink contains 50g sunflower oil and vehicle (almond milk, chocolate drink powder, sweetener)

干预措施: Test drink (Other)

Fat Test drink (38g)

Experimental

This drink contains 38g sunflower oil and vehicle (almond milk, chocolate drink powder, sweetener)

干预措施: Test drink (Other)

Fat Test drink (13g)

Experimental

This drink contains 13g sunflower oil and vehicle (almond milk, chocolate drink powder, sweetener)

干预措施: Test drink (Other)

Fat Test drink (3g)

Placebo Comparator

This drink contains no sunflower oil and vehicle (almond milk, chocolate drink powder, sweetener)

干预措施: Test drink (Other)

Carbohydrate Test drink

Active Comparator

This drink contains 20g of glucose from de-gassed lucozade energy.

干预措施: Test drink (Other)

结局指标

主要结局

Glycaemic excursion

时间窗: During the 8 hours post drink

The mean glucose excursion from fasting (measured by CGMS) at each 30 minute interval over the 8 hour postprandial period for each test condition

次要结局

  • Maximal glucose excursion(During the 24h post drink)
  • Percent time in target glucose range(During the 24h post drink)
  • Time to maximal glucose excursion(During the 8 hours post drink)
  • Time until the glucose level returns to baseline(During the 8 hours post drink)
  • Number of hypoglycaemic events in the 24h post-test meal(During the 24 hours post drink)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Susan O'Connell

Consultant Paediatric Endocrinologist

Cork University Hospital

研究点 (1)

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