Insulin Dosage Software Program for People With Type 1 and Type 2 Diabetes

Diabetes Clinical Trial

Official title:

Open-Label, Uncontrolled, Single-Arm, Single-Center, 16-Week Study Assessing Efficacy and Safety of Frequently Modified Insulin Therapy Using Dosage Recommending Device Software in 3-Groups of Subjects With Diabetes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01170208
• Other study ID #: 03985-10-A
• Secondary ID: R41DK085974
• Status: Completed
• Phase: N/A
• Start date: June 2010
• Est. completion date: March 2011

Study information

• Verified date: January 2014
• Source: HealthPartners Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to determine the effectiveness and safety of the computer software program in providing insulin dosage recommendations. Participation in the study for 60 research subjects will last for 16-weeks and includes 3-4 clinic visits and a series of weekly telephone calls from the study team (minimum of 12 calls). Participants will be provided with weekly Study Log Sheets to record their daily blood glucose readings, insulin doses, grams of carbohydrate eaten at each meal (if they have type-1 diabetes) and any changes in their health (e.g., hypoglycemic episodes, illnesses). Participants will fax or drop off a copy of the Study Log Sheet. This information will be entered by the IDC study team into the computer software program. The IDC study team will review the information from the software and, based on the IDC's study team approval, any insulin dose changes will be communicated back to the patient by phone or fax.

Description:

Hygieia, Inc. is developing a device intended for use by insulin-requiring patients with diabetes. It will be a pocket-sized, hand-held device, combining a glucose meter with software that analyzes blood glucose levels recorded in the device's memory, and periodically recommends modifications in insulin dosage. The already developed software algorithms are based on the way an endocrinologist evaluates and frequently adjusts insulin dosage in a patient with diabetes.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 46
• Est. completion date: March 2011
• Est. primary completion date: March 2011
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years to 70 Years

Eligibility

Inclusion Criteria:

• GROUP I

• Have been clinically diagnosed with type-1 diabetes for at least 1-year

• Have an HgbA1c of 7.4% or higher

• Treated with short-acting insulin analog (i.e. HumaLog® Lispro, NovoLog® Aspart, Apidra® Glulisine) before each meal and only one injection of long-acting insulin analog Lantus® (Glargine), per day. Subjects must typically eat 3 meals per day. The total daily combined dose of the long-acting and short-acting insulin analogs must be 25 units or more. Patient must have been using the same insulin regimen for the previous 3-months

• Is currently using an insulin/carbohydrate ratio to decide how much short-acting insulin to take before meals and must be able to use the gram versus choice method of carbohydrate counting.

• GROUP II

• Have been clinically diagnosed with type-2 diabetes for at least 1-year

• Have an HgbA1c of 7.4% or higher

• Treated with short-acting insulin analog (i.e. HumaLog® Lispro, NovoLog® Aspart, Apidra® Glulisine) before each meal and only one injection of long-acting insulin analog Lantus® (Glargine) per day and. Subjects must typically eat 3 meals per day. The total daily combined dose of the long-acting and short-acting insulin analogs must be 25 units or more. Patient must have been using the same insulin regimen for the previous 3-months

• May be using other diabetes agent(s) at a stable dose for the last 3-months.

• GROUP III

• Have been clinically diagnosed with type-2 diabetes for at least 1-year

• Have an HgbA1c of 7.8% or higher

• Take twice daily biphasic Insulin (e.g. HumaLog® Mix 75/25, NovoLog® Mix 70/30) or premixed insulin (i.e. Humulin® 70/30, Novolin® 70/30, NPH/Regular insulin 70/30) with a total daily insulin dose of 25 units and have been using the same insulin regimen for the past 3-months

• May be using other diabetes agent(s) at a stable dose for the last 3-months.

Exclusion Criteria:

• Have a history of greater than 2 episodes of severe hypoglycemia in the past year, or have hypoglycemic unawareness when glucose levels are less than or equal to 50 mg/dl

• Have a significant physical, psychological, or cognitive impairment that would prohibit adherence to the protocol

• Have any severe cardiovascular disease including a history of congestive heart failure (New York Heart Association [NYHA] 3 or 4), unstable angina, myocardial infarction or stroke that occurred within the 6-months preceding enrollment

• Have known active anemia with a hemotocrit less than 25% in women or 30% in men

• Have known history of renal disease (e.g., serum creatinine level >2.0 mg/dl or eGFR < 30 ml/min)

• Have active cancer or cancer in the past 2-years (except non-melanoma skin cancer

• Have history of significant liver disease including cirrhosis or elevated liver enzymes (e.g., AST and ALT greater than 3 times the upper limit of normal values)

• Have a body mass index (BMI) > 45 kg/m2; and/or

• Are pregnant, plan to become pregnant during the study period, or are breastfeeding.

Related Conditions & MeSH terms

• Diabetes
• Diabetes Mellitus
• Insulin

Intervention

Device:
• insulin dose software
The rationale to conduct this study is that Hygieia hypothesizes the software will effectively and safely optimize glucose control in insulin-requiring patients with type-1 and type-2 diabetes. The software was designed to provide safe insulin dosage recommendations.

Locations

Country	Name	City	State
United States	International Diabetes Center	Minneapolis	Minnesota

Sponsors (5)

Lead Sponsor	Collaborator
HealthPartners Institute	Hygieia, Inc, International Diabetes Center at Park Nicollet, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

References & Publications (3)

Bergenstal RM, Johnson M, Powers MA, Wynne A, Vlajnic A, Hollander P, Rendell M. Adjust to target in type 2 diabetes: comparison of a simple algorithm with carbohydrate counting for adjustment of mealtime insulin glulisine. Diabetes Care. 2008 Jul;31(7):1305-10. doi: 10.2337/dc07-2137. Epub 2008 Mar 25. — View Citation

Diabetes Control and Complications Trial Research Group, Nathan DM, Genuth S, Lachin J, Cleary P, Crofford O, Davis M, Rand L, Siebert C. The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med. 1993 Sep 30;329(14):977-86. — View Citation

Herman WH, Ilag LL, Johnson SL, Martin CL, Sinding J, Al Harthi A, Plunkett CD, LaPorte FB, Burke R, Brown MB, Halter JB, Raskin P. A clinical trial of continuous subcutaneous insulin infusion versus multiple daily injections in older adults with type 2 diabetes. Diabetes Care. 2005 Jul;28(7):1568-73. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Weekly Mean Blood Glucose From Week 4 to Week 16		Twelve week period from week 4 to week 16
Secondary	Reduction in HbA1c.		Twelve week period from week 4 to week 16
Secondary	Reduction in Fructosamine.		12 week period from Week 4 to Week 16
Secondary	Incidence of Severe or Serious Hypoglycemia.		January 2011

External Links

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