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临床试验/NCT03717896
NCT03717896已完成2 期

Thiamine as Adjunctive Therapy for Diabetic Ketoacidosis

Beth Israel Deaconess Medical Center2 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2018年11月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
102
试验地点
2
主要终点
plasma bicarbonate levels

研究概览

简要总结

This is a randomized, double-blind, placebo-controlled trial to determine if administration of intravenous thiamine will lead to quicker resolution of acidosis in patients admitted to the hospital with diabetic ketoacidosis. The investigators will secondarily investigate whether thiamine improves cellular oxygen consumption, shortens intensive care unit (ICU) and hospital stay or decreases hospital resource utilization.

详细描述

Thiamine (vitamin B1) is a water-soluble vitamin that plays a key role in aerobic glucose metabolism. Thiamine is a cofactor of pyruvate dehydrogenase (PDH), an enzyme that must be activated for entry into the Krebs Cycle for aerobic metabolism. PDH activity is reduced in thiamine deficient states, resulting in a shift in pyruvate metabolism to the anaerobic pathway. This leads to increased lactate production and acidosis. Thiamine loss in the urine, with consequent thiamine deficiency, is not uncommon in diabetes. The investigators' preliminary studies have found that thiamine deficiency in occurs in as many as 39% of patients with DKA, and that thiamine levels are inversely associated with lactate and acidosis. The investigator hypothesizes that treating DKA patients with intravenous thiamine will lead to faster resolution of acidosis and improved aerobic metabolism. The investigator's secondary hypothesis is that thiamine treatment will shorten stays in the ICU and hospital and lead to utilization of fewer hospital resources.

In this randomized, double-blind, placebo-controlled trial, patients admitted to the hospital with DKA who are enrolled in the study will be randomized to either intravenous thiamine (200mg in 0.9% saline) twice daily for two days or an identical volume of 0.9% saline on the same schedule. The investigator's primary outcome is change in bicarbonate over the 24 hours following enrollment, with measurements at 0, 6, 12, 18, 24 hours, using a linear mixed-effects model. Secondarily, patients will be stratified by Type I and Type II DM. Additionally, a pre-planned sub-analysis of thiamine deficient subjects will be performed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • Bicarbonate ≤15 mEq/L
  • Anion gap > 12 mEq/L
  • Blood pH≤ 7.24 (if already obtained by clinical team)
  • Urine ketones (qualitative) or serum ketones (β-hydroxybutyric acid) > 3 mmol/L
  • Enrollment within 6 hours of presentation

排除标准

  • Current thiamine supplementation ≥ 6 milligrams per day (i.e., more than a multivitamin)
  • Competing causes of severe acidosis including seizure, carbon monoxide poisoning, cyanide toxicity, cardiac arrest, liver dysfunction (specifically defined as known cirrhosis)
  • Known allergy to thiamine
  • Competing indication for thiamine administration as judged by the clinical team (e.g., significant alcohol use)
  • Research-protected populations (pregnant women and prisoners)
  • Patient enrolled previously in same study
  • Code status of Do Not Resuscitate/Do Not Intubate (DNR/DNI) or Comfort Measures Only (CMO)

研究组 & 干预措施

Thiamine

Experimental

200mg IV thiamine in 50mL 0.9% saline twice daily for 2 days

干预措施: 200mg IV thiamine in 50mL 0.9% saline (Drug)

Placebo

Placebo Comparator

100mL 0.9% saline twice daily for two days

干预措施: Placebo (Drug)

结局指标

主要结局

plasma bicarbonate levels

时间窗: 24 hours

Our primary outcome is change in bicarbonate over the 24 hours following enrollment with measurements at 0, 6, 12, 18, 24 hours using a linear-effects model

次要结局

  • oxygen consumption by circulating mononuclear cells(24 hours)
  • anion gap(24 hours)
  • lactate(24 hours)
  • ICU length of stay(24 hours)
  • hospital resource usage(24 hours)
  • hospital length of stay(24 hours)

研究者

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

Michael Donnino

Associate Professor of Medicine and Emergency Medicine

Beth Israel Deaconess Medical Center

研究点 (2)

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