Comparison of Exenatide and Metformin Monotherapy in Overweight/Obese Patients With Newly Diagnosed Type 2 Diabetes
Primary Purpose
Type2 Diabetes
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Exenatide or metformin hydrochloride
Sponsored by

About this trial
This is an interventional treatment trial for Type2 Diabetes
Eligibility Criteria
Inclusion Criteria:
- age 20 - <65 years,
- body mass index (BMI) ≥ 24 kg/m2,
- HbA1c ≥ 7% (53mmol/mol).
- diabetes antibodies (-)
- diagnosed with T2D within the previous 3 months
Exclusion Criteria:
- anti-diabetic drugs or diet therapy before participation
- pancreatitis
- coronary artery disease
- liver function impairment
- renal function impairment
- intestinal surgery
- chronic hypoxic diseases (emphysema and cor pulmonale)
- infectious disease
- hematological disease
- systemic inflammatory disease
- cancer
- pregnant, possibly pregnant
- ingesting agents known to influence glucose or lipid metabolism
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
exenatide group
metformin group
Arm Description
The drug-naïve, overweight or obese patients with newly diagnosed T2D
The drug-naïve, overweight or obese patients with newly diagnosed T2D
Outcomes
Primary Outcome Measures
The change of HbA1c
Secondary Outcome Measures
Full Information
NCT ID
NCT03297879
First Posted
September 26, 2017
Last Updated
September 29, 2017
Sponsor
Beijing Chao Yang Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03297879
Brief Title
Comparison of Exenatide and Metformin Monotherapy in Overweight/Obese Patients With Newly Diagnosed Type 2 Diabetes
Official Title
Beijing Chao-Yang Hospital, Capital Medical University
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
January 1, 2013 (Actual)
Primary Completion Date
February 28, 2016 (Actual)
Study Completion Date
February 28, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing Chao Yang Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The present study assessed the therapeutic effect of exenatide and metformin as the initial therapy in overweight/obese patients with newly diagnosed Type 2 diabetes (T2D).
Detailed Description
The present study was a prospective, nonrandomized, interventional study.The drug-naïve, overweight or obese patients with newly diagnosed T2D were consecutively enrolled. The inclusion criteria: 1) age 20 - <65 years, 2) body mass index (BMI) ≥ 24 kg/m2 [7], and 3) HbA1c ≥ 7% (53mmol/mol). An oral glucose tolerance test was performed during the screenings. All of the patients have no diabetes antibodies and were diagnosed with T2D within the previous 3 months, according to the ADA diagnostic criteria. None of the patients had administered anti-diabetic drugs or diet therapy before participation. Neither of the patients presented any history of pancreatitis, coronary artery disease, liver function impairment, renal function impairment, intestinal surgery, chronic hypoxic diseases (emphysema and cor pulmonale), infectious disease, hematological disease, systemic inflammatory disease, or cancer. Patients who were pregnant, possibly pregnant, or ingesting agents known to influence glucose or lipid metabolism were also excluded.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type2 Diabetes
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
230 (Actual)
8. Arms, Groups, and Interventions
Arm Title
exenatide group
Arm Type
Experimental
Arm Description
The drug-naïve, overweight or obese patients with newly diagnosed T2D
Arm Title
metformin group
Arm Type
Active Comparator
Arm Description
The drug-naïve, overweight or obese patients with newly diagnosed T2D
Intervention Type
Drug
Intervention Name(s)
Exenatide or metformin hydrochloride
Intervention Description
Exenatide was administrated with 5 μg bid for 4 weeks and 10 μg bid for 8 weeks. Metformin hydrochloride was initiated at a dose of 500 mg bid for 2 weeks, and added to 2.0 g/day for 8 weeks.
Primary Outcome Measure Information:
Title
The change of HbA1c
Time Frame
baseline and 12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age 20 - <65 years,
body mass index (BMI) ≥ 24 kg/m2,
HbA1c ≥ 7% (53mmol/mol).
diabetes antibodies (-)
diagnosed with T2D within the previous 3 months
Exclusion Criteria:
anti-diabetic drugs or diet therapy before participation
pancreatitis
coronary artery disease
liver function impairment
renal function impairment
intestinal surgery
chronic hypoxic diseases (emphysema and cor pulmonale)
infectious disease
hematological disease
systemic inflammatory disease
cancer
pregnant, possibly pregnant
ingesting agents known to influence glucose or lipid metabolism
12. IPD Sharing Statement
Citations:
PubMed Identifier
35432194
Citation
Zhang L, Hu Y, An Y, Wang Q, Liu J, Wang G. The Changes of Lipidomic Profiles Reveal Therapeutic Effects of Exenatide in Patients With Type 2 Diabetes. Front Endocrinol (Lausanne). 2022 Mar 31;13:677202. doi: 10.3389/fendo.2022.677202. eCollection 2022.
Results Reference
derived
PubMed Identifier
29358950
Citation
Liu J, Hu Y, Xu Y, Jia Y, Miao L, Wang G. Comparison of Exenatide and Metformin Monotherapy in Overweight/Obese Patients with Newly Diagnosed Type 2 Diabetes. Int J Endocrinol. 2017;2017:9401606. doi: 10.1155/2017/9401606. Epub 2017 Nov 20.
Results Reference
derived
Learn more about this trial
Comparison of Exenatide and Metformin Monotherapy in Overweight/Obese Patients With Newly Diagnosed Type 2 Diabetes
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