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临床试验/NCT03644199
NCT03644199撤回不适用

Factors Responsible for the Development of Diabetes in Adults With Cystic Fibrosis

Liverpool Heart and Chest Hospital NHS Foundation Trust1 个研究点 分布在 1 个国家开始时间: 2011年3月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Glucose levels

研究概览

简要总结

This is a crossover study to determine the possible factors that might be related to the development of diabetes in CF and examines the relationship between pancreatic fatigue if any, and the development of diabetes. In addition hormones affecting the release of insulin and stomach motility will be studied to determine if there is a variation in response to solid and liquid meals and if this variation increases as fatigue progresses.

详细描述

The main purpose of this study is to look at possible additional factors that might be related to the development of Cystic Fibrosis Related Diabetes (CFRD), that in itself is a unique entity and to identify an appropriate test to diagnose CFRD. There is well demonstrated evidence of delayed insulin release and peak in individuals with CF, the cause of which is not fully explained.

With a view to determine the cause of this phenomenon the aims of this study are:

  1. To determine whether pancreatic fatigue contributes to this delayed insulin release and peak that is seen in patients with cystic fibrosis.
  2. Should a glucose tolerance test be done at a later time in the day, as against first thing in the morning as is the current accepted standard?
  3. To determine if gastric emptying has a role to play in the development of CFRD?
  4. To study the hormone release response to a glucose challenge and the patterns of change through the day.
  5. To study the relationship of these hormones to gastric emptying and the development of diabetes.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •In order to participate in the study, the CF group must meet all the following inclusion criteria
  • •Male or female with a confirmed diagnosis of cystic fibrosis defined by
  • •Clinical features consistent with a diagnosis of CF AND
  • •Sweat chloride ≥60mmol/L by pilocarpine ionotophoresis; OR
  • •Genotypic confirmation of CFTR mutation
  • •Aged 18 - 50 years
  • •Out-patients from the regional adult unit in Liverpool
  • •Currently not known to be diabetic or on insulin
  • •Clinically stable over the preceding 4 weeks i.e. no indication for iv antibiotics, steroids or hospital admissions
  • •Hemoglobin value >10g/dl
  • •The inclusion criteria for the normal population group is as follows:
  • •Male or female with NO confirmed diagnosis of cystic fibrosis
  • •Aged 18 - 50 years
  • •Currently not known to be diabetic or on insulin
  • •Clinically stable over the preceding 4 weeks i.e. no indication for iv antibiotics, steroids or hospital admissions
  • •Hemoglobin value >10g/dl
  • •In order to participate subjects must not meet any of the following

排除标准

  • •Patients with known diabetes or on glucose lowering medications (insulin, oral agents)
  • •On-going acute illness
  • •Those on long-term oral steroids
  • •Pregnant women
  • •Those on immunosuppressive treatment
  • •History of, or planned organ transplant
  • •Clinically significant abnormal findings on haematology or clinical chemistry
  • •Subjects with documented or suspected, clinically significant, alcohol or drug abuse. The determination of clinical significance will be determined by the investigator.
  • •Current malignant disease
  • •Any serious or active medical or psychiatric illness, which in eth opinion of the investigator, would interfere with subject treatment, assessment, or compliance with the protocol.

研究组 & 干预措施

OGTT test

Other

Comparison of responses to a OGTT between CF subjects and health control subjects

干预措施: Oral Glucose Tolerance Test (OGTT) assessment arm (Other)

Mixed meal

Other

Comparison of responses to a mixed meal through the day between CF subjects and health control subjects

干预措施: Mixed meal test evaluation test arm (Other)

结局指标

主要结局

Glucose levels

时间窗: 4 hours

Glucose sensitivity test

次要结局

  • Insulin responses(4 hours)
  • Evaluation of gastric emptying(8 hours)
  • GLP1 and GIP responses(4 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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