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临床试验/jRCT1022240017
jRCT1022240017已完成不适用

Evaluation of the artificial intelligence (AI) for predicting optimized insulin dosage in diabetic patients

Renascience Inc.0 个研究点目标入组 130 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
130
主要终点
Correct rate

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • Clinical data of hospitalized type 2 diabetes patients who received insulin therapy from diabetologists will be collected, provided they meet all the following eligibility criteria and do not fall under any exclusion criteria.
  • Eligibility Criteria:
  • (1) Patients using ultra-rapid-acting insulin and long-acting insulin (insulin glargine, insulin degludec)
  • (2) Patients aged 20 years or older
  • (3) Patients who have provided written consent to participate in the study
  • (4) Patients with a hospital stay of 7 days or more

排除标准

  • (1) Patients who are pregnant or may be pregnant
  • (2) Patients with or suspected of having diabetic gastroparesis
  • (3) Patients with severe diabetic autonomic neuropathy
  • (4) Patients with pre-proliferative diabetic retinopathy or proliferative diabetic retinopathy, or suspected of having these conditions
  • (5) Patients undergoing continuous subcutaneous insulin infusion therapy or continuous intravenous insulin infusion
  • (6) Patients who have not been discharged since undergoing general anesthesia surgery
  • (7) Patients with missing data in the specified input data without any reason such as tests
  • (8) Patients whose primary purpose is not blood glucose control
  • (9) For cases from Tohoku University Hospital, data from hospitalizations before 2021 (as these data may have been used for the training of the experimental device)

结局指标

主要结局

Correct rate

Rate when the difference between the test device and the units prescribed by diabetologists is within the acceptable range.

次要结局

未报告次要终点

研究者

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