Effects of Liraglutide on the Cognitive Function in Patients With Type 2 Diabetes Mellitus
Primary Purpose
Type 2 Diabetes Mellitus
Status
Completed
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Liraglutide
placebo
Sponsored by

About this trial
This is an interventional treatment trial for Type 2 Diabetes Mellitus focused on measuring Type 2 diabetes mellitus, Cognitive function, Liraglutide
Eligibility Criteria
Inclusion Criteria:
- Type 2 diabetes。
Exclusion Criteria:
- 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.
Sites / Locations
- The third hospital affiliated to the Third Military Medical University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Liraglutide
Placebo
Arm Description
12 weeks of liraglutide treatment at adjusting dose, up to 1.8mg/day Drug: liraglutide
12 weeks of Placebo treatment at adjusting dose Drug:Placebo
Outcomes
Primary Outcome Measures
Changes of cognitive function assessed by cognitive function scale after 12 weeks.
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.
Secondary Outcome Measures
Changes of systolic blood pressure and diastolic blood pressure
Change of systolic blood pressure and diastolic blood pressure compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of fasting plasma glucose
Change of fasting plasma glucose compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of HbA1c
Change of HbA1c compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of lipid profile
Change of lipids profiles (TC, HDL-C, LDL-C, TG) in mmol/L compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of liver enzymes
Change of liver enzymes (ALT, AST in IU/L) compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of kidney function
Change of kidney function(serum creatinine in umol/L、eGFR in ml/min) compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of CRP
Change of CRP compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of Body mass index(BMI)
Change of Body mass index(BMI) compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of waist circumference
Change of waist circumference compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of hip circumference
Change of hip circumference compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Change of waist-to-hip ratio
Change of waist-to-hip ratio compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Full Information
NCT ID
NCT03707171
First Posted
September 27, 2018
Last Updated
July 9, 2019
Sponsor
Third Military Medical University
1. Study Identification
Unique Protocol Identification Number
NCT03707171
Brief Title
Effects of Liraglutide on the Cognitive Function in Patients With Type 2 Diabetes Mellitus
Official Title
Effects of Liraglutide on the Cognitive Function in Patients With Type 2 Diabetes Mellitus
Study Type
Interventional
2. Study Status
Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
October 1, 2018 (Actual)
Primary Completion Date
February 1, 2019 (Actual)
Study Completion Date
May 1, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Third Military Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus
Keywords
Type 2 diabetes mellitus, Cognitive function, Liraglutide
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Liraglutide
Arm Type
Active Comparator
Arm Description
12 weeks of liraglutide treatment at adjusting dose, up to 1.8mg/day Drug: liraglutide
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
12 weeks of Placebo treatment at adjusting dose Drug:Placebo
Intervention Type
Drug
Intervention Name(s)
Liraglutide
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
Any hypoglycemic drugs except glucagon-like peptide type 1 (GLP-1) analogue.
Primary Outcome Measure Information:
Title
Changes of cognitive function assessed by cognitive function scale after 12 weeks.
Description
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.
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Secondary Outcome Measure Information:
Title
Changes of systolic blood pressure and diastolic blood pressure
Description
Change of systolic blood pressure and diastolic blood pressure compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of fasting plasma glucose
Description
Change of fasting plasma glucose compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of HbA1c
Description
Change of HbA1c compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of lipid profile
Description
Change of lipids profiles (TC, HDL-C, LDL-C, TG) in mmol/L compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of liver enzymes
Description
Change of liver enzymes (ALT, AST in IU/L) compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of kidney function
Description
Change of kidney function(serum creatinine in umol/L、eGFR in ml/min) compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of CRP
Description
Change of CRP compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of Body mass index(BMI)
Description
Change of Body mass index(BMI) compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of waist circumference
Description
Change of waist circumference compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of hip circumference
Description
Change of hip circumference compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
Title
Change of waist-to-hip ratio
Description
Change of waist-to-hip ratio compared with baseline, and between the intervention and control group at the end of the study (12 weeks)
Time Frame
Baseline,4weeks,8weeks,12weeks(End of Trial)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Type 2 diabetes。
Exclusion Criteria:
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.
Facility Information:
Facility Name
The third hospital affiliated to the Third Military Medical University
City
Chongqing
State/Province
Chongqing
ZIP/Postal Code
400042
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
34250817
Citation
Li Q, Jia M, Yan Z, Li Q, Sun F, He C, Li Y, Zhou X, Zhang H, Liu X, Bu X, Gao P, He H, Zhao Z, Zhu Z. Activation of Glucagon-Like Peptide-1 Receptor Ameliorates Cognitive Decline in Type 2 Diabetes Mellitus Through a Metabolism-Independent Pathway. J Am Heart Assoc. 2021 Jul 20;10(14):e020734. doi: 10.1161/JAHA.120.020734. Epub 2021 Jul 10.
Results Reference
derived
Learn more about this trial
Effects of Liraglutide on the Cognitive Function in Patients With Type 2 Diabetes Mellitus
We'll reach out to this number within 24 hrs