Effect of Short-Term Intensive Insulin Sequential Exenatide Therapy in Newly Diagnosed Type 2 Diabetic Patients
Primary Purpose
Diabetes Mellitus, Type 2
Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
insulin lispro injection, exenatide injection
insulin lispro injection
Sponsored by

About this trial
This is an interventional treatment trial for Diabetes Mellitus, Type 2
Eligibility Criteria
Inclusion Criteria:
- newly-diagnosed type 2 diabetic patients, drug naïve
- age 30~70 years
- FPG 7.0~16.7mmol/L
- BMI 20~35 kg/m2, stable body weight (≤10% variation) for at least 3 months prior to screening
- female patients of reproductive age should practice a reliable method of birth control throughout the study
Exclusion Criteria:
- acute or severe chronic diabetic complications
- Recently suffered from MI or CVA.
- severe gastrointestinal disease
- other severe intercurrent illness
- serum aminotransferase (ALT and AST) level higher than 2 times of the upper normal limits and/or serum creatinie≥133µmol/L (1.5mg/dL)
- tested positive for glutamic acid decarboxylase antibody
- use of weight loss drugs, corticosteroids, drugs known to affect gastrointestinal motility, transplantation medications, or any investigational drug
- history of pancreatitis
- Pregnant or lactation women.
Sites / Locations
- The first afilliated hospital of Xiamen university
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
insulin lispro injection, exenatide injection
insulin lispro injection
Arm Description
Outcomes
Primary Outcome Measures
the glycemic remission rate in different groups
Secondary Outcome Measures
the improvement of β-cell function in different groups.
the time of glycemic remission in different groups
Full Information
NCT ID
NCT01776788
First Posted
January 22, 2013
Last Updated
March 8, 2015
Sponsor
The First Affiliated Hospital of Xiamen University
1. Study Identification
Unique Protocol Identification Number
NCT01776788
Brief Title
Effect of Short-Term Intensive Insulin Sequential Exenatide Therapy in Newly Diagnosed Type 2 Diabetic Patients
Official Title
Effect of Short-Term Intensive Insulin Sequential Exenatide Therapy on β-cell Function and Glycemic Remission Rate in Newly Diagnosed Type 2 Diabetic Patients
Study Type
Interventional
2. Study Status
Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
August 2012 (undefined)
Primary Completion Date
February 2015 (Actual)
Study Completion Date
February 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The First Affiliated Hospital of Xiamen University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The randomized, controlled trial is to investigate and evaluate the effects of short-term continuous subcutaneous insulin infusion (CSII) sequential exenatide therapy on β-cell function, long-term glycemic control and glycemic remission rate in newly diagnosed type 2 diabetic patients.
Detailed Description
The UK Prospective Diabetes Study has shown that β-cell function progressively deteriorates over time in people with type 2 diabetes mellitus, irrespective of lifestyle and existing pharmacological interventions. The progressive nature of type 2 diabetes is one of the major challenges in the treatment of affected patients, and agents that could alter the natural history of this condition would add greatly to current treatment approaches. Short-term intensive insulin therapy of newly diagnosed type 2 diabetes will improve beta-cell function and usually leading to a temporary remission time. The effect of GLP-1 receptor agonists on beta-cells is stimulation of glucose-dependent insulin release, followed by enhancement of insulin biosynthesis. It is stimulating beta-cell proliferation, induction of islet neogenesis, and inhibition of ß-cell apoptosis. Exenatide is synthetic exendin-4, GLP-1 receptor agonist. Exenatide exerts direct effects on β-cell, which indicates that may contribute to delay disease progression. However, no study has evaluated effect of short-term intensive insulin sequential exenatide therapy model on β-cell function and glycemic remission rate in newly diagnosed type 2 diabetic patients. This current study is thus designed to evaluate effect of short-term intensive insulin sequential exenatide therapy model on β-cell function , glycemic control and glycemic remission rate in newly diagnosed type 2 diabetic patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
156 (Actual)
8. Arms, Groups, and Interventions
Arm Title
insulin lispro injection, exenatide injection
Arm Type
Experimental
Arm Title
insulin lispro injection
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
insulin lispro injection, exenatide injection
Intervention Description
First, Patients in the exenatide group will receive short-term continuous subcutaneous insulin (CSII)therapy. The doses will be titrated every day in order to attain the glycaemic goal which is defined as a fasting capillary blood glucose of less than 6.1 mmol/L and capillary blood glucose at 2 h after each of three meals of less than 8.0 mmol/L. Treatments will be maintained for 2 weeks after the glycaemic target will be reached. Then, patients will Sequential be treated with 5 mcg bid for 4 weeks and then 10 mcg bid for 8 weeks. After interventions will be stopped, patients will be instructed to continue diet and physical exercise only and will be followed-up with glycaemic monitoring monthly
Intervention Type
Drug
Intervention Name(s)
insulin lispro injection
Intervention Description
Patients in the control group will receive insulin with an insulin pump. The doses will be titrated every day in order to attain the glycaemic goal. Treatments will be maintained for 2 weeks after the glycaemic target will be reached. Then interventions will be stop, patients will be instructed to continue diet and physical exercise only and will be followed-up with glycaemic monitoring monthly.
Primary Outcome Measure Information:
Title
the glycemic remission rate in different groups
Time Frame
one year
Secondary Outcome Measure Information:
Title
the improvement of β-cell function in different groups.
Time Frame
one year
Title
the time of glycemic remission in different groups
Time Frame
one year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
newly-diagnosed type 2 diabetic patients, drug naïve
age 30~70 years
FPG 7.0~16.7mmol/L
BMI 20~35 kg/m2, stable body weight (≤10% variation) for at least 3 months prior to screening
female patients of reproductive age should practice a reliable method of birth control throughout the study
Exclusion Criteria:
acute or severe chronic diabetic complications
Recently suffered from MI or CVA.
severe gastrointestinal disease
other severe intercurrent illness
serum aminotransferase (ALT and AST) level higher than 2 times of the upper normal limits and/or serum creatinie≥133µmol/L (1.5mg/dL)
tested positive for glutamic acid decarboxylase antibody
use of weight loss drugs, corticosteroids, drugs known to affect gastrointestinal motility, transplantation medications, or any investigational drug
history of pancreatitis
Pregnant or lactation women.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xue-jun Li, MD,PhD
Organizational Affiliation
The First Affiliated Hospital of Xiamen University, China
Official's Role
Study Director
Facility Information:
Facility Name
The first afilliated hospital of Xiamen university
City
Xiamen
State/Province
Fujian
ZIP/Postal Code
361003
Country
China
12. IPD Sharing Statement
Learn more about this trial
Effect of Short-Term Intensive Insulin Sequential Exenatide Therapy in Newly Diagnosed Type 2 Diabetic Patients
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