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临床试验/NCT02318966
NCT02318966已完成不适用

A Comparison of Glycosade® and Uncooked Cornstarch (UCCS) for the Dietary Management of Hepatic Glycogen Storage Diseases (GSD)

Vitaflo International, Ltd10 个研究点 分布在 4 个国家目标入组 61 人开始时间: 2016年2月22日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
61
试验地点
10
主要终点
To assess if Glycosade® will result in improved blood glucose, lactate and ketone levels in a larger group of patients with GSD I, III, VI & IX as measured by duration of normal blood glucose levels or prevention of ketosis

研究概览

简要总结

To compare efficacy of Glycosade® with uncooked corn starch (UCCS for the dietary management of hepatic glycogen storage diseases (GSD).

详细描述

'Glyde' is a prospective, randomised, double-blind, crossover trial to compare the effects of two different starches used in the dietary management of GSD.

The study will recruit 64 patients from six centres in the UK, USA, France and The Netherlands. The planned duration per participant is 2 years.

Participants will be randomised into two equally sized groups:

Arm A- Glycosade intake given first, followed by UCCS 1-6 weeks later Arm B- UCCS intake given first, followed by Glycosade 1-6 weeks later.

The objective of this trial is to establish whether Glycosade® improves outcomes for patients with GSD compared to UCCS therapy by comparing the duration of normal blood sugars, lactate and ketone levels of patients with hepatic GSD (Types I, III, VI and IX) post equivalent intakes of UCCS and Glycosade®.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
2 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed by either genetic mutation analysis or enzymology study (this includes patients with only a single mutation but who also have supportive enzymology consistent with the condition). For those whom mutation analysis is not completed this will be assessed during the study.
  • Aged 2 years or older (5 years or older in the USA)
  • Established on full intake of uncooked corn starch therapy for at least 6 months

排除标准

  • Women who are pregnant or breastfeeding at the start of the study or planning to become pregnant during the study will be excluded.
  • children less than 2 years of age

结局指标

主要结局

To assess if Glycosade® will result in improved blood glucose, lactate and ketone levels in a larger group of patients with GSD I, III, VI & IX as measured by duration of normal blood glucose levels or prevention of ketosis

时间窗: 24 hours

次要结局

  • 1. The insulin area under the curve during dietary management with UCCS compared to dietary management with Glycosade®.(24 hours)
  • 2. The area under the curve in lactate, BOHB, during dietary management with UCCS compared to dietary management with Glycosade®.(24 hours)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (10)

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