Status:
TERMINATED
Connected Pens for Diabetes Study
Lead Sponsor:
Companion Medical, Inc.
Conditions:
Diabetes Mellitus
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The objective of the study is to evaluate the impact of a wireless smart insulin pen and smartphone-based bolus advisor on clinical and psychosocial outcomes in insulin-treated diabetes mellitus patie...
Detailed Description
The study is a prospective, randomized, controlled treatment design. The study device will be used for multiple daily injection (MDI) therapy of insulin. The participant will interact with the study d...
Eligibility Criteria
Inclusion
- The participant is ≥ 18 years of age
- The participant has Type 1 OR Type 2 diabetes and is being treated with intensive insulin therapy via injection for ≥ 3 months. Intensive insulin therapy is defined as at least one long acting insulin dose and two or more short acting insulin doses per day.
- Glycated hemoglobin (HbA1c) ≥ 7.5%).
- The participant is a current iPhone user for over 30 days.
- Participant adjusts meal insulin doses based on carbohydrate content of meals.
- The participant is fluent in the English language.
- The participant and the investigator understand participant obligations and agree that the participant is willing and able to complete the study visits.
- Patients prandial insulin need must be \<30 U per meal.
Exclusion
- The participant has been using unblinded CGM for less than 6 months.
- The participant uses pre-mixed insulin.
- Current use of a smart insulin pen.
- Use of sliding scale insulin therapy that determines insulin dosages based exclusively on specific blood glucose results
- Used systemic oral or inhaled steroids for more than 7 days within the last 3 months
- Oral anti-diabetic agents, with the exception of metformin
- Injectable anti-diabetic agents other than insulin
- The participant is legally blind or has below specified best-corrected vision level.
- Diagnosed with any clinically significant infectious disease or major organ system disease, such as gastroparesis or renal disease (at Investigator's discretion)
- The participant is pregnant, lactating, or plans to become pregnant in the next 6 months.
- The participant is currently participating in another clinical study that may preclude the participant from meeting the obligations of this study.
- The participant has any additional condition(s) (medical, social, or psychosocial) that in the investigator's opinion would warrant exclusion from the study or prevent the participant from completing or complying with the study requirements.
Key Trial Info
Start Date :
May 30 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 12 2019
Estimated Enrollment :
21 Patients enrolled
Trial Details
Trial ID
NCT03830216
Start Date
May 30 2019
End Date
November 12 2019
Last Update
January 27 2021
Active Locations (1)
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1
Mary & Dick Allen Diabetes Center, Hoag Memorial Hospital Presbyterian
Newport Beach, California, United States, 92663