Efficacy Comparison of Polyethylene Glycol Loxenatide and Gliclazide on the Brain Function in T2DM Patients

NARecruitingINTERVENTIONAL
Enrollment

58

Participants

Timeline

Start Date

May 10, 2020

Primary Completion Date

February 29, 2024

Study Completion Date

June 30, 2024

Conditions
Type 2 Diabetes MellitusCognitive Function Abnormal
Interventions
DRUG

loxenatide Group

Loxenatide will be initiated and maintained at 0.2mg once weekly until the completion of the study. All patients will also continue on their existing dose and regimen of metformin throughout the study.

DRUG

Gliclazide Group

Gliclazide will be initiated and maintained at 30mg/day every morning. If necessary, the dose can be increased to 120mg once daily. All patients will also continue on their existing dose and regimen of metformin throughout the study.

Trial Locations (1)

210008

RECRUITING

Division of Endocrinology, the Affiliated Drum Tower Hospital of Nanjing University, Nanjing

All Listed Sponsors
lead

The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

OTHER