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临床试验/NCT03659383
NCT03659383Unknown4 期

The Exploration of Optimal Treatment Scheme in Patients With Type 2 Diabetes Inadequately Controlled With Glargine

Nanjing First Hospital, Nanjing Medical University0 个研究点目标入组 100 人开始时间: 2018年9月20日最近更新:
适应症
干预措施

试验速览

阶段
4 期
入组人数
100
主要终点
Rate of reaching target of glucose

研究概览

简要总结

Glargine is commonly used in insulin supplemental therapy in patients with type 2 diabetes(T2D) at present. However, many patients who treated with glargine still have poor blood glucose control because of insufficient insulin dose or improper oral medication. This study aims to investigate the optimal treatment scheme in order to improve the blood control in these patients. Continuous Glucose Monitoring System (CGMS) will be used to assess the blood glucose control at baseline and the moment when the patients achieved standard. Oral medications will be standardized first, and insulin doses will be adjusted according to blood glucose values obtained by self-monitoring. Glycemic control will be considered as reaching target of glucose if the fasting capillary blood glucose is less than 6.1 mmol/L. The maximum period of blood glucose adjustment will be 1 months. Oral medication, the type and dosage of insulin, exercise status, insulin injection skill evaluation, islet function, duration of diabetes, complications and insulin antibodies will be recorded in detail at baseline, reaching target of glucose standard and 3 months after reaching target of glucose.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with T2DM, which was defined bypublished Criteria of World Health Organization in 1999;
  • Patients were using glargine with or without oral hypoglycemic drugs and having a stable dose of glargine for more than 2 month would be recruited into this study;
  • Patients had relatively constant diet and exercise in 2 month before the study.
  • Fasting blood glucose was between 6.1 and 16mmolL, and postprandial (or random) blood glucose <22.2mmol/L

排除标准

  • Patients with severe cardiovascular diseases, such as stroke, transient ischemic attack, myocardial infarction, unstable angina, coronary artery bypass grafting, percutaneous coronary intervention, and heart failure;
  • Patients with severe infectious diseases;
  • Patients with acute complications of diabetes on admission, such as diabetic ketoacidosis, diabetic hyperosmolar nonketotic coma, and lactic acidosis;
  • Patients with history of psychiatric disorders and were unsuitable to use CGMS;
  • Any other situations that made patients unsuitable to participate in the study, such as alcoholism and drug abuse.

研究组 & 干预措施

Optimal hypoglycemic treatment

Experimental

The patients will receive optimal hypoglycemic treatments, including adjustment of insulin dose and oral antidiabetic agents

干预措施: Optimal hypoglycemic treatment (Combination Product)

结局指标

主要结局

Rate of reaching target of glucose

时间窗: 0-1 month

Rate of reaching target of glucose

次要结局

  • HbA1c(0-3 month)
  • Dosage of insulin(0-1 month)
  • Time of reaching target of glucose(0-1 month)

研究者

申办方类型
Other
责任方
Sponsor

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