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临床试验/NCT06206525
NCT06206525已完成不适用

Feasibility Trial Using an Insulin Dosing Calculator for Patients With Type 2 Diabetes Mellitus on Hospital Admission

University of Washington5 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2024年3月22日最近更新:
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
38
试验地点
5
主要终点
Clinical significant hypoglycemia

研究概览

简要总结

The goal of this feasibility trial is to test whether a novel insulin dosing calculator can improve blood glucose management for patients with type 2 diabetes mellitus on hospital admission. The main questions it aims to answer are:

  • Whether using this calculator leads to no excessive hypoglycemia?
  • Whether using this calculator leads to a decrease of hyperglycemia?

Participants will receive initial insulin doses by the calculator on hospital admission, and the rest of care will follow standard of care. Participants will be compared with patients in the UW observational cohort who received initial insulin doses by standard of care.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Patients who are admitted to University of Washington Medical Centers
  • With history of type 2 and/or steroid-induced diabetes mellitus
  • Receiving insulin therapy prior to admission

排除标准

  • Patients who are admitted to ICU or obstetrics ward
  • Patients who are admitted for elective surgery or procedure
  • Patients who present with diabetic ketone acidosis, hyperosmolar hyperglycemic state or require intravenous insulin infusion
  • Patients who have no meal intake for 24 hours prior to admission, or planned nothing per oral (NPO) during the first 24 hours after admission
  • Patients who report low appetite (25% or less) on admission or have a significantly decreased level of consciousness that study team does not think they are going to eat right after admission
  • Patients who receive enteral feeding after admission
  • Patients who develop severe acute kidney injury needing dialysis therapy

研究组 & 干预措施

Initial insulin dosing calculator

Experimental

干预措施: Initial insulin dosing calculator (Other)

Observational cohort

No Intervention

Historical patients who received initial insulin doses by standard of care

结局指标

主要结局

Clinical significant hypoglycemia

时间窗: During the first 48 hours after admission

Participates who develop blood glucose concentration lower than 54 mg/dL

Clinical Significant Hypoglycemia

时间窗: During the first 48 hours after admission

Participates developed blood glucose concentration lower than 54 mg/dL

次要结局

  • Mean blood glucose concentration (mg/dL)(During the first 24 hours after admission)
  • Hypoglycemia lower than 70 mg/dL(During the first 48 hours after admission)
  • Clinical significant hyperglycemia(During the first 48 hours after admission)
  • Mean Blood Glucose Concentration (mg/dL)(During the first 24 hours after admission)
  • Clinical Significant Hyperglycemia(During the first 48 hours after admission)
  • Hypoglycemia Lower Than 70 mg/dL(During the first 48 hours after admission)

研究者

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

Hou-Hsien Chiang

Clinician researcher

University of Washington

研究点 (5)

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