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临床试验/EUCTR2017-003088-36-PL
EUCTR2017-003088-36-PL
进行中(未招募)
1 期

GPPAD-POInT (Global Platform of Autoimmune Diabetes – Primary Oral Insulin Trial)Oral Insulin Therapy for Prevention of Autoimmune Diabetes - GPPAD-POInT (Global Platform of Autoimmune Diabetes – Primary Oral Insulin Trial)

Technische Universität München, Represented by the school of medicine0 个研究点目标入组 1,040 人2017年10月30日

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
未指定
发起方
Technische Universität München, Represented by the school of medicine
入组人数
1040
状态
进行中(未招募)
最后更新
8年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2017年10月30日
结束日期
待定
最后更新
8年前
研究类型
Interventional clinical trial of medicinal product
性别
All

研究者

发起方
Technische Universität München, Represented by the school of medicine

入排标准

入选标准

  • 1\. Infant between the ages of 4 months and 7 months at the time of randomization.
  • 2\. A high genetic risk (\>10%) to develop beta\-cell autoantibodies by age 6 years:
  • A) For infants without a first degree family history of type 1 diabetes, high genetic risk is defined as a DR3/DR4\-DQ8 or DR4\-DQ8/DR4\-DQ8 genotype, and a genetic risk score that is \>14\.4\.
  • B) For infants with a first degree family history of type 1 diabetes, high genetic risk is defined as having HLA DR4 and DQ8, and none of the following protective alleles: DRB1\*1501, DQB1\*0503\.
  • 3\. Solid foods introduced into diet of infant
  • 4\. Written informed consent signed by the custodial parent(s).
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 1040
  • F.1\.2 Adults (18\-64 years) no
  • F.1\.2\.1 Number of subjects for this age range

排除标准

  • 1\. Concomitant disease or treatment that may interfere with the assessments, as judged by the investigators.
  • 2\. Any condition that could be associated with poor compliance.
  • 3\. Any medical condition or medical condition coexisting, which, in the opinion of the investigator, may jeopardize the participant’s safe participation in the study.
  • 4\. Diagnosis of diabetes at the time of recruitment.
  • 5\. Participation in another clinical trial.

结局指标

主要结局

未指定

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