Adjunctive Metformin Therapy in Double Diabetes

Diabetes Mellitus Clinical Trial

— AMTIDD  

Official title:

Glycemic Control in Children and Adolescents With Double Diabetes: Trial of Optimized Insulin-Metformin Regimen

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01334125
• Other study ID #: 13938
• Status: Completed
• Phase: Phase 3
• First received: March 21, 2011
• Last updated: March 3, 2016
• Start date: February 2011
• Est. completion date: December 2014

Study information

• Verified date: March 2016
• Source: University of Massachusetts, Worcester
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The significance of this project is to investigate the effects of adjunctive metformin therapy in children and adolescents with double diabetes. Double diabetes describes a clinical state where an individual possesses features of both type 1 and type 2 diabetes. There is a paucity of data on the role of adjunctive metformin therapy in children and adolescents with double diabetes. To help fill this knowledge gap, the investigators propose a randomized, double-blind, placebo-controlled trial of metformin in double diabetes. Specifically, the investigators will evaluate changes in hemoglobin A1c and anthropometry in patients with a diagnosis of type 1 diabetes who also have features of type 2 diabetes or metabolic syndrome as well as patients with type 2 diabetes who possess diabetes-associated autoantibodies. This will help determine the safety profile, and efficacy of adjunctive metformin therapy in these subjects.

Description:

In this 12-month clinical trial, a 3-month run-in period will precede the interventional phase of the study. All patients will be placed on treat-to-target insulin regimen alone during the run-in phase. At the end of the 3-month run-in period, all participants will continue on treat-to-target insulin regimen, and will then be randomized to either of the 2 arms of the study: an experimental arm, consisting of treat-to-target insulin regimen plus metformin, and a control arm consisting of treat-to-target insulin regimen plus placebo. Both the physicians and patients will be blinded to the oral agents being administered to patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: December 2014
• Est. primary completion date: December 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 10 Years to 20 Years

Eligibility

Inclusion Criteria:

A. General inclusion criteria

1. Ten to 20 years of age.

2. Pubertal (Tanner stages 2-5, by examination).

3. Hemoglobin A1c level of > 8.0% in the 6 months prior to enrollment.

4. All subjects must have access to a computer.

B. Specific inclusion criteria: [Subjects could have either #1, or #2].

1. Subjects with clinical and biochemical features of T2DM of > 6mo duration who also have positive T1DM antibodies

• Clinical features: acanthosis nigricans, BMI >85%

• Biochemical: evidence of insulin resistance at diagnosis

• fasting insulin >27 uIU/mL(normal range 6-27) at a fasting blood glucose of = 126 mg/dL, or

• fasting c-peptide level of > 7.1 ng/mL (normal range 0.9 - 7.1), or

• Homeostasis model of insulin resistance of >3.16

2. Patients with T1DM of > one yr duration with BMI >85%

• Presentation with ketoacidosis at diagnosis

• C-peptide <0.9 ng/mL (normal range 0.9 - 7.1),or (insulin < 6 uIU/mL) (NR 6-27) at diagnosis (when blood glucose is = 126 mg/dL)

• Can be antibody positive or negative

• Increased insulin requirement (>2 Units/kg/day)

Exclusion Criteria:

1. Subjects on weight altering medications, such as orlistat.

2. Subjects with eating disorder

3. Subjects on medications other than insulin and or metformin that may affect blood glucose level.

4. Subjects with abnormal hepatic function tests.

5. Subjects with nephropathy, defined in this case as an overnight albumin excretion rate of >200 mcg/min using a first morning urine sample collection.

6. Subjects with recurrent diabetes ketoacidosis (more than 2 episodes in the past 12 months), or recurrent severe hypoglycemia (more than 2 episodes of hypoglycemia with altered level of consciousness, requiring assistance to treat in the past year).

7. Pregnant, breast-feeding or the intention of becoming pregnant or not using adequate contraceptive measures.

8. Known or suspected allergy to metformin.

9. The receipt of any investigational drug within 6 months prior to this trial.

10. Active malignant neoplasms.

11. No access to a computer.

12. Subjects currently taking metformin for clinical purposes are not eligible to be enrolled in this study.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetes Mellitus

Intervention

Drug:
• Metformin
Metformin 1000 mg once daily by mouth for 9 months
• Placebo
2 capsules once daily by mouth for 9 months

Locations

Country	Name	City	State
United States	UmassMemorial Medical Center	Worcester	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
University of Massachusetts, Worcester

Country where clinical trial is conducted

United States, 

References & Publications (1)

Nwosu BU, Maranda L, Cullen K, Greenman L, Fleshman J, McShea N, Barton BA, Lee MM. A Randomized, Double-Blind, Placebo-Controlled Trial of Adjunctive Metformin Therapy in Overweight/Obese Youth with Type 1 Diabetes. PLoS One. 2015 Sep 14;10(9):e0137525. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Baseline Adjusted Hemoglobin A1c Over Time	Comparison of the baseline-adjusted differences in HbA1c between the metformin and placebo groups during the trial. Hemoglobin A1c is a marker of glycemic control. The reported values represented means adjusted for baseline values, age, gender, and BMI using repeated measures ANOVA (General Linear Model).	Baseline, 3mo, 6mo, and 9 months	No
Secondary	Baseline Adjusted Changes in Lipid Profile Over Time	Comparison of the baseline-adjusted differences in total cholesterol/high density cholesterol index over time between the metformin and the placebo groups. The reported values represented means adjusted for baseline values, age, gender, and BMI using repeated measures ANOVA (General Linear Model).	Baseline, 3mo, 6mo, and 9 months	No
Secondary	Baseline Adjusted Changes in Adiponectin/Leptin Ratio Over Time	Comparison of the baseline-adjusted differences in adiponectin/leptin ratio over time between the metformin and the placebo groups. The reported values represented mean adjusted for baseline values, age, gender, and BMI using repeated measures ANOVA (General Linear Model).	Baseline, 3mo, 6 mo, and 9 months	No
Secondary	Number of Participants With Minor, Major, and Nocturnal Hypoglycemia	Comparison of the occurrence of hypoglycemic event requiring a third party assistance (major hypoglycemia) per subject during the study, and minor hypoglycemia (plasma glucose of <60 mg/dL or no measurement), as well as nocturnal hypoglycemia (plasma glucose of =60 mg/dL between 11PM and 6AM).	12 months	Yes