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临床试验/NCT03707171
NCT03707171已完成3 期

Effects of Liraglutide on the Cognitive Function in Patients With Type 2 Diabetes Mellitus

Third Military Medical University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018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
状态
已完成
入组人数
30
试验地点
1
主要终点
Changes of cognitive function assessed by cognitive function scale after 12 weeks.

研究概览

简要总结

Type 2 diabetes mellitus (T2DM) can impaire cognitive function,the prevalence of Alzheimer's Disease(AD) in T2DM patients is 1.5 to 2.5 times higher than the general population.Cognitive impairment seriously affects the health and quality of life of the elderly. Prevention and treatment measures for cognitive decline in persons with T2DM has not been well studied.

Glucagon-like peptide-1 (GLP-1) is a member of an endogenous class of incretin hormones synthesized in intestinal epithelial L-cells.GLP-1 enhances glucose-dependent secretion of insulin,inhibits glucagon secretion, slows gastric emptying and reduces food intake. Liraglutide is a glucagon-like peptide type 1 (GLP-1) analogue. It has been proved that Liraglutide can improve insulin resistance and cognitive function in AD animals. Therefore, it is speculated that Liraglutide may interfere with the occurrence and development of cognitive dysfunction in patients with T2DM. In order to confirm the effects, the investigators conduct an open, prospective, positive controlled study in patients with T2DM. The effect on BMI,waist circumference, hip circumference, waist-to-hip ratio,fasting plasma glucose,glycosylated hemoglobin,blood lipids and cognitive function were measured to explore the effects of liraglutide in patients with T2DM.

The overall goal of this study is to explore the effects of liraglutide on the cognitive function in patients with type 2 diabetes mellitus and make further contribution to the improvement of cognitive function.

研究设计

研究类型
Interventional
分配方式
Non 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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Type 2 diabetes。

排除标准

  • Type 2 diabetes with acute diabetic complications.
  • Type 1 diabetes.
  • Other diseases affecting cognitive function (congenital dementia,brain trauma,severe heart dysfunction,severe kidney dysfunction,severe lung dysfunction,epilepsy,severe hypoglycemic coma,cerebrovascular disease,ischemic heart disease,etc).
  • Alcohol abuse,mental illness and psychoactive substance abuse.
  • History of thyroid disease.
  • Any surgical or medical conditions that significantly influence absorption, distribution, metabolism or excretion of the intervention drugs.

研究组 & 干预措施

Placebo

Placebo Comparator

12 weeks of Placebo treatment at adjusting dose Drug:Placebo

干预措施: placebo (Drug)

Liraglutide

Active Comparator

12 weeks of liraglutide treatment at adjusting dose, up to 1.8mg/day Drug: liraglutide

干预措施: Liraglutide (Drug)

结局指标

主要结局

Changes of cognitive function assessed by cognitive function scale after 12 weeks.

时间窗: Baseline,4weeks,8weeks,12weeks(End of Trial)

The cognitive function will be calculated from performance on the following measures: (1)Digit Span Test(DST);(2) Rey Auditory Verbal Learning(RAVL);(3) Long-Delay Free Recall(LDFR);(4) Trail Making Test(TMT);(5) Animal Naming Test(ANT);(6) Clock Drawing Test(CDT);(7)Minimum Mental State Examination(MMSE);(8)Memory and executive screening(MES);(8)functional near-infrared spectroscopy.

次要结局

  • Changes of systolic blood pressure and diastolic blood pressure(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of fasting plasma glucose(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of HbA1c(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of lipid profile(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of liver enzymes(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of kidney function(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of CRP(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of Body mass index(BMI)(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of waist circumference(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of hip circumference(Baseline,4weeks,8weeks,12weeks(End of Trial))
  • Change of waist-to-hip ratio(Baseline,4weeks,8weeks,12weeks(End of Trial))

研究者

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

Zhiming Zhu

Director of the department of Hypertension & Endocrinology, Daping Hospital

Third Military Medical University

研究点 (1)

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