Type 1 Diabetes
Conditions
Brief summary
The purpose of this study is to collect data on the feasibility of the HLCL system in a camp setting.
Detailed description
This study is a single-arm, single-center, in clinic Investigation in subjects with type 1 diabetes on insulin pump therapy. Run-in Period A total of up 10 subjects will be enrolled (age 18-25). A minimum of 6 days run-in period with the 640G (sensor augmented pump) will be used to collect sensors and insulin data and to allow the subject to become familiar. Study Period - Camp Following the run-in period subjects will participate in a 5 day, 4 night study period in an camp setting during which the CL feature will be studied. Subjects will receive 3 meals each day, one night they receive a high fat dinner, one morning they will receive breakfast high in carbohydrates. Subjects will be asked to exercise for up to 60 minutes on one day during their study period. Subjects will be asked to take a minimum of 5 fingersticks a day (before each meal, morning and before bedtime)
Interventions
DEVICEHybrid-logic closed loop system
All patients get to wear the pump
Sponsors
Medtronic Diabetes
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Diabetes duration \> 1 year since diagnosis 2. Sensor augmented Pump for at least 6 months 3. Age 18-25 4. A1C \<10.0 at time of screening visit 5. Willing to follow study instructions 6. Willing to perform ≥ 5 finger stick blood glucose measurements daily 7. Willing to perform required sensor calibrations 8. Patient capable of reading and understand instructions in English
Exclusion criteria
1. Subject is unable to tolerate tape adhesive in the area of sensor placement 2. Subject has any unresolved adverse skin condition in the area of sensor or device placement (e.g., psoriasis, rash, Staphylococcus infection) 3. Subject is actively participating in an investigational study (drug or device) wherein they have received treatment from an investigational study (drug or device) in the last 2 weeks 4. Subject has a positive pregnancy screening test 5. Subject is female, sexually active without the use of contraception, and plans/able to become pregnant during the course of the study and is not using an acceptable method of contraception 6. Subject has had a hypoglycemic seizure within the past 6 months prior to screening visit 7. Subject has had hypoglycemia resulting in loss of consciousness within the past 6 months prior to screening visit 8. Subject has had an episode of diabetic ketoacidosis (DKA) within the past 6 months prior to screening visit 9. Subject has a history of a seizure disorder 10. Subject has central nervous system or cardiac disorder resulting in syncope 11. Subject has a history of myocardial infarction, unstable angina, coronary artery bypass surgery, coronary artery stenting, transient ischemic attack (TIA), cerebrovascular accident (CVA), angina, congestive heart failure, ventricular rhythm disturbances or thromboembolic disease 12. Subjects with hematocrit lower than the normal reference range per POC or local lab testing 13. Subjects with a history or findings on screening electrocardiogram (EKG) of any cardiac arrhythmia, including atrial arrhythmias 14. Subjects with a history of adrenal insufficiency 15. Subjects with history of migraines that have occurred at least 2 times in the last 3 months prior to enrollment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Descriptive endpoints | after 4 days of camp | Time in different range SG 70 mg/dL ≤ SG ≤ 180 mg/dL |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Descriptive endpoints | after 4 days of camp | Serious Adverse Events (SAE) |
Outcome results
None listed