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临床试验/NCT03051243
NCT03051243Unknown3 期

Safety and Efficacy of Linagliptin Therapy in the Setting of Internal Medicine Department Type 2 Diabetes Mellitus

Rabin Medical Center0 个研究点目标入组 60 人开始时间: 2017年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
入组人数
60
主要终点
Percentage of patient with mean blood glucose levels

研究概览

简要总结

Prospective, open labels, randomized study. A total of 60 admitted patient between 18 and 85 years old with known with history of DM for more than 3 months and an average of two consecutive blood glucose levels above 180 mg/dl (after stopping all previous oral antidiabetic and insulin on admission) will be enrolled Patient will be randomized to a 1:1 ratio in two treatment groups regimens- linagliptin (trajenta) once daily combined with basal insulin at bed time (glargine Lantus; sanofi) and basal bolus insulin with glargine once daily and glulisine (Apidra; sanifi) before meals.

Patient will be discharged according to discharged protocol. Follow-up visits will take place at 3 and 6 months post discharged.

详细描述

patient in the linagliptin plus basal insulin will receive linagliptin at single dose of 5 mg/day, and a starting total daily dose (TDD) of glargine of 0.3 units/kg/day, while patients >70 years of age and/or with a serum creatinine >2.0 mg/dL will receive starting TDD of 0.15 units/kg.

Patient in the basal bolus group will start at a TDD of 0.5 units/kg divided half as insulin glargine once daily and half as insulin glulisine before meals. In patients >70 years of age and/or with a serum creatinine >2.0 mg/dL, the starting TDD will be reduce to 0.3 units/kg.

The results of BG values will be measured as 2 hour pre meal glucose, bedtime glucose, and mean daily BG after first day at hospital, HbA1c will be measured on the first day of hospitalization.

Patient with pre-meal and bed time blood glucose levels over 180 mg/dl will receive correctional doses of short acting insulin based on glucose levels as follow- 180-250mg/dl 2 units of insulin, 250-300 mg/dl 3 units of insulin, 350-400 4 units of insulin.

Hypoglycemic events shall be documented as well. In case of treatment failure, defined as average blood glucose levels or two consecutive measurements of more than 240 mg/dl, patient's treatment will be changed to basal based regimen.Patient with pre-meal and bed time blood glucose levels over 180 mg/dl will receive correctional doses of short acting insulin based on glucose levels as follow- 180-250mg/dl 2 units of insulin, 250-300 mg/dl 3 units of insulin, 350-400 4 units of insulin.

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
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male & female patient with Known history of DM for more than 3 months before randomization.
  • Hospital admission due to blood glucose levels ranging between 180-400 mg/dl.
  • Average of two consecutive blood glucose levels above 180 mg/dl.
  • Age between 18 and 85 years old.
  • Home treatment with diet alone, any combination of oral antidiabetic agents, or insulin therapy at daily dose <0.4 units/kg.

排除标准

  • BG >400 mg/dl in the period before randomization.
  • Prior history of hyperglycemic crises.
  • Have hyperglycemia without history of diabetes.
  • Patient who expected ICU admission or cardiac surgery.
  • A history of pancreatitis, active gallbladder disease, Corticosteroid therapy or hepatic disease.
  • Impaired renal function (glomerular filtration rate [GFR] <30 mL/min or serum creatinine ≥3.0 mg/dL).
  • History of diabetic ketoacidosis.
  • Pregnancy.
  • Inability to give informed consent (poor mental status).

研究组 & 干预措施

Linagliptin and Basal Insulin

Active Comparator

linagliptin (trajenta) 5mg once daily combined with basal insulin (glargine Lantus; sanofi) 0.15-0.3 units/kg TDD before bed time.

干预措施: Linagliptin and Basal Insulin (Drug)

Basal Insulin and Bolus Insulin

Active Comparator

Basal Insulin (Glargine Lantus; Sanofi) based therapy once daily before bedtime and glulisine (Apidra; sanofi) before meals. insulin dose will be 0.5 units/kg divided half as insulin glargine once daily and half as insulin glulisine before meals.

干预措施: Basal Insulin and Bolus Insulin (Drug)

结局指标

主要结局

Percentage of patient with mean blood glucose levels

时间窗: After firts day from admission and Up to 14 days, 3 and 6 month after discharge.

between 80-180 mg/dl.

次要结局

  • Difference in BG values within range(After firts day from admission and Up to 14 days, 3 and 6 month after discharge)
  • Number of hypoglycemic events (BG <70 and or < 40 mg/dL).(After firts day from admission and Up to 14 days, 3 and 6 month after discharge)
  • Number of episodes of hyperglycemia(After firts day from admission and Up to 14 days, 3 and 6 month after discharge)
  • TTD (total daily dose) of insulin(After firts day from admission and Up to 14 days, 3 and 6 month after discharge)

研究者

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

Dror Dicker

Head of internal medicine D' and obesity clinic

Rabin Medical Center

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