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Effects of Sitagliptin on Type 2 Diabetes Mellitus Patients on Treatment With Metformin and Insulin

Primary Purpose

Diabetes Mellitus, Type 2

Status
Completed
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
Sitagliptin
Glimepiride
Metformin
Insulin
Sponsored by
Jothydev's Diabetes and Research Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2 focused on measuring Diabetes Mellitus, Type 2, Sitagliptin, Insulin

Eligibility Criteria

25 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • T2DM patients on metformin and biphasic or basal regimens of insulin
  • HbA1c ≥7.3% to ≤8.5%
  • Age: 25 to 60 yrs
  • Insulin TDD > 10 IU

Exclusion Criteria:

  • Use of acarbose, pioglitazone or short-acting insulin analogues at time of run-in phase
  • History of type 1 diabetes mellitus
  • Creatinine clearance ≤50 mL/min
  • Chronic liver & kidney diseases, SGOT/PT≥2.5x upper limit of normal, uncontrolled thyroid disorders , cardiac failure, hemochromatosis, autoimmune disorders, corticosteroid intake.
  • BMI >40 kg/m2

Sites / Locations

  • Jothydev's Diabetes and Research Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Sitagliptin along with metformin and insulin

Glimepiride as an active comparator to Sitagliptin

Arm Description

Outcomes

Primary Outcome Measures

Reduction in HbA1c from baseline
To confirm the efficacy of metformin+ insulin+ sitagliptin in controlling glycemia with respect to change from baseline in HbA1c after 24 weeks of administration. This will be accomplished by comparing the difference in change from baseline in HbA1c after 24 weeks of administration, compared with metformin+insulin+glimepiride to a non-inferiority limit of 0.3% , and if non-inferiority is proven, to a superiority limit of 0%.

Secondary Outcome Measures

Change in total daily dose (TDD) of insulin
Change from baseline in insulin TDD (30-day geometric mean) at Month 6
Episodes of hypoglycemia
Hypoglycemia (Total, severe, nocturnal) (From Month 0 to Month 6), as assessed by questionnaire and supplemented by SMBG values, if available
Proportion of patients with HbA1c reduction
Proportion of patients, who completed treatment , with HbA1c value <6.5% & ≤7.3% at end of study (Month 6)
change in weight and BMI
Change in both HbA1c and TDD
Proportion of patients achieving both HbA1c ≤6.5% AND reduction in TDD (total daily dose of insulin)
Change in insulin resistance and beta cell function
Change from baseline in c-peptide levels, homeostasis model assessments of β-cell function and insulin resistance (HOMA-β and HOMA-IR)
Change in lipid profile from baseline

Full Information

First Posted
April 23, 2011
Last Updated
May 29, 2014
Sponsor
Jothydev's Diabetes and Research Centre
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1. Study Identification

Unique Protocol Identification Number
NCT01341717
Brief Title
Effects of Sitagliptin on Type 2 Diabetes Mellitus Patients on Treatment With Metformin and Insulin
Official Title
Open-labelled, Randomized, Active-controlled, Parallel-arm, Single-center Study on Effect of Sitagliptin on T2DM Patients on Treatment With Metformin and Insulin
Study Type
Interventional

2. Study Status

Record Verification Date
May 2014
Overall Recruitment Status
Completed
Study Start Date
February 2012 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Jothydev's Diabetes and Research Centre

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to determine the efficacy and safety of sitaglipin in the treatment of Type 2 diabetes mellitus (T2DM) patients with inadequate glycemic control using metformin and insulin.
Detailed Description
DPP-4 inhibitors enhance function of endogenous incretin that helps with glucose homoeostasis. DPP-4 inhibitors have been proved to promote glycemic control without increasing risk of hypoglycemia and weight gain. In addition, they may improve beta-cell function and do not have any known associations with overt cardiovascular or hepatic safety risks. Addition of sitagliptin to treatment of T2DM patients poorly controlled on insulin +/- metformin has been shown to reduce HbA1c while being generally well-tolerated. It could be clinically useful to add sitaglipin to treatment regimen of T2DM patients on stable therapy with insulin & metformin. Apart from glycemic reduction, secondary effects like prevention of weight gain, reduction in insulin dose, improved cardiovascular risk profile, etc. may be expected from addition of sitagliptin to treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2
Keywords
Diabetes Mellitus, Type 2, Sitagliptin, Insulin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
440 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sitagliptin along with metformin and insulin
Arm Type
Experimental
Arm Title
Glimepiride as an active comparator to Sitagliptin
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Sitagliptin
Intervention Description
100 mg once daily for 6 months
Intervention Type
Drug
Intervention Name(s)
Glimepiride
Intervention Description
1 mg/2 mg/3 mg once daily
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
>=1000 mg twice daily
Intervention Type
Drug
Intervention Name(s)
Insulin
Intervention Description
TDD > 10 IU once/twice daily
Primary Outcome Measure Information:
Title
Reduction in HbA1c from baseline
Description
To confirm the efficacy of metformin+ insulin+ sitagliptin in controlling glycemia with respect to change from baseline in HbA1c after 24 weeks of administration. This will be accomplished by comparing the difference in change from baseline in HbA1c after 24 weeks of administration, compared with metformin+insulin+glimepiride to a non-inferiority limit of 0.3% , and if non-inferiority is proven, to a superiority limit of 0%.
Time Frame
six months
Secondary Outcome Measure Information:
Title
Change in total daily dose (TDD) of insulin
Description
Change from baseline in insulin TDD (30-day geometric mean) at Month 6
Time Frame
6 months
Title
Episodes of hypoglycemia
Description
Hypoglycemia (Total, severe, nocturnal) (From Month 0 to Month 6), as assessed by questionnaire and supplemented by SMBG values, if available
Time Frame
6 months
Title
Proportion of patients with HbA1c reduction
Description
Proportion of patients, who completed treatment , with HbA1c value <6.5% & ≤7.3% at end of study (Month 6)
Time Frame
6 months
Title
change in weight and BMI
Time Frame
6 months
Title
Change in both HbA1c and TDD
Description
Proportion of patients achieving both HbA1c ≤6.5% AND reduction in TDD (total daily dose of insulin)
Time Frame
6 months
Title
Change in insulin resistance and beta cell function
Description
Change from baseline in c-peptide levels, homeostasis model assessments of β-cell function and insulin resistance (HOMA-β and HOMA-IR)
Time Frame
6 months
Title
Change in lipid profile from baseline
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: T2DM patients on metformin and biphasic or basal regimens of insulin HbA1c ≥7.3% to ≤8.5% Age: 25 to 60 yrs Insulin TDD > 10 IU Exclusion Criteria: Use of acarbose, pioglitazone or short-acting insulin analogues at time of run-in phase History of type 1 diabetes mellitus Creatinine clearance ≤50 mL/min Chronic liver & kidney diseases, SGOT/PT≥2.5x upper limit of normal, uncontrolled thyroid disorders , cardiac failure, hemochromatosis, autoimmune disorders, corticosteroid intake. BMI >40 kg/m2
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jothydev Kesavadev, MD
Organizational Affiliation
Jothydev's Diabetes and Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jothydev's Diabetes and Research Center
City
Thiruvananthapuram
State/Province
Kerala
ZIP/Postal Code
695032
Country
India

12. IPD Sharing Statement

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Effects of Sitagliptin on Type 2 Diabetes Mellitus Patients on Treatment With Metformin and Insulin

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