A Study of Technology to Improve Glucose Control in Participants With Type 1 Diabetes
Completed
Conditions studied: Diabetes Mellitus, Type 1
In brief
The main purpose of this study is to determine whether combining meal, glucose, and insulin data in a web-based system will improve management of type 1 diabetes (T1D). No study drug will be given. The study will last about 18 weeks.
Key facts
- Study ID
- NCT03758430
- Run by
- Eli Lilly and Company
- People needed
- 28
- Starts
- 2019-02-06
- Expected to finish
- 2020-08-07
- Last updated by the study team
- 2020-08-21
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- T1D by clinical diagnosis for > 3 years
- Insulin pump use > 3 months: must use one of the following pump types: Animas Ping and Vibe, Insulet Omnipod, Medtronic 523/723 and 530G, Tandem t:slim and t:flex
- Continuous Glucose Monitor (CGM) > 3 months and current use of Dexcom G5 at least 6 out of 7 days per week
- HbA1c 7.0-9.5%
- Must have iPhone (meal-tagging app has been built on iOS)
- Personal computer for uploading of pump and CGM devices
- Willingness to follow study protocol including tagging food data
- Comfort speaking, reading, and writing English
You may not qualify if…
- Individuals currently using a hybrid closed-loop system (e.g., Medtronic 670G)
- Individuals planning to follow a specific diet plan for weight loss
- Inability to consume "common meals"
- Gastroparesis;
- Eating disorder
- Evidence of missed insulin meal-time insulin boluses on pump download
- Use of medications that can affect blood glucose levels (such as SGLT inhibitors, steroid, beta agonists)
- Use of medications that affect gastric emptying (such as GLP agonists, pramlinitide)
- Alcohol abuse
- Pre-conception, pregnancy, or lactation
Where it is running
- Joslin Diabetes Center — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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