Status:

COMPLETED

Effect of Dulaglutide on Glycemic Variability in Patients With Type 2 Diabetes

Lead Sponsor:

Shanghai Zhongshan Hospital

Conditions:

Type 2 Diabetes

Eligibility:

All Genders

18-70 years

Brief Summary

Glycemic variability will be assessed using continuous glucose monitor(CGM) in type 2 diabetic patients who receive dulaglutide 1.5 mg/qw injection for 4 weeks.

Detailed Description

Glycemic fluctuation is a major problem in glucose control in diabetic patients. It is interesting to know that whether weekly GLP-1RA can improve glycemic variability in diabetic patients. The presen...

Eligibility Criteria

Inclusion

  • Fully understand the test content and possible adverse reactions and voluntarily participate in the trial and sign the informed consent form;
  • Meet the World Health Organization(WHO) (1999) criteria for the diagnosis and classification criteria for type 2 diabetes;
  • 18 ≤ age ≤ 70 years old, male or female;

Exclusion

  • Subjects with Type 1 diabetes mellitus or secondary diabetes mellitus (i.e. any type other than T2DM)
  • Personal history or family history of thyroid medullary carcinoma or multiple endocrine neoplasia type 2 (MEN2).
  • History of pancreatitis or considered clinically at significant risk of developing pancreatitis during the course of the study (e.g. due to symptomatic gallstones).
  • History of significant gastrointestinal (GI) surgery that in the opinion of the investigator is likely to significantly affect upper GI or pancreatic function.
  • Fasting triglyceride level more than 750 mg/dL at screening.
  • Estimated Glomerular Filtration Rate (eGFR) less than 60 mL/minute/1.73 meter\^2 (calculated using the Schwartz equation) at screening.
  • ALT more than 2.5x upper limit of normal (ULN) or Bilirubin more than 1.5xULN (isolated bilirubin more than 1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin more than 35%) at screening.
  • Use of a GLP-1receptor agonist at study entry and during the study.

Key Trial Info

Start Date :

May 8 2020

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

June 30 2021

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT04374578

Start Date

May 8 2020

End Date

June 30 2021

Last Update

March 31 2022

Active Locations (1)

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Page 1 of 1 (1 locations)

1

180 Fenglin Road

Shanghai, China, 200032