| Eligibility |
Inclusion Criteria
1. Age 18-85 years, BMI = 18.5, have had clinical type 1 diabetes for at least one year,
and have taken insulin for at least 1 year
1. Prescription diabetes medication regimen stable for > 1 month, including any
adjunctive anti-diabetic medications (except for medications that will not affect
the safety of the study and are not expected to affect any outcome of the study,
in the judgment of the site principal investigator)
2. This does not include changes to any insulin doses, including basal
rates/long-acting insulin doses, carbohydrate to insulin ratios and correction
factors
2. Willing to wear one Dexcom CGM transmitter and sensor (sensor must be changed every 10
days), and one infusion set that must be replaced at least every 3 days.
3. Endocrinology practice criterion is that diabetes is managed using sensor-augmented
insulin pump therapy or artificial pancreas therapy for = 3 months)
4. Primary care practice criteria are that diabetes is managed by multiple daily insulin
injections (insulin-pump naïve).
5. TH group criterion is that participant must have hardware and internet access capable
of 2-way video and audio communication
Exclusion Criteria
1. Unable to provide informed consent (e.g. impaired cognition or judgment)
2. Unable to safely comply with study procedures and reporting requirements (e.g.
impairment of vision or dexterity that prevents safe operation of the bionic pancreas,
impaired memory)
3. Unable to speak and read English, as iLet BP support materials and device menus are
currently available in English only.
4. Plan to change usual diabetes regimen in the next 3 months including before and during
participation in the study
1. This would include changing from MDI to pump or from pump to MDI, and starting a
CGM if not previously used
2. This would not include changes to any insulin doses, including basal rates/long
acting insulin doses, carbohydrate to insulin ratios and correction factors
5. Current use of non-FDA approved closed-loop or hybrid closed-loop insulin delivery
system (e.g. "Loop" or "Open APS")
6. Unwilling to switch to lispro or aspart for the duration of the study's iLet arm (e.g.
from Fiasp or Lyumjev)
7. Known hemoglobinopathy (sickle cell trait is not an exclusion)
8. Current participation in another diabetes-related clinical trial, has a medical
condition, or use of a medication that, in the judgment of the investigator, could
compromise the results of this study or the safety of the participant
9. History of diabetes due to cystic fibrosis, pancreatitis, or other pancreatic disease,
including pancreatic tumor or insulinoma, or history of complete pancreatectomy
10. Have a history of intermittently required glucocorticoid treatment (e.g., but not
limited to, for the treatment of asthma, inflammatory bowel disease).
11. A1c >11.0% (most recent value up to 1 year prior acceptable; if none available or >1
year prior, participant will be instructed to obtain A1c through their usual care
provider and to make copy of result available to study team)
12. History of diabetic ketoacidosis (DKA) within the past month
13. Electrically powered implants (e.g. cochlear implants, neurostimulators) that might be
susceptible to RF interference
14. Established history of allergy or severe reaction to adhesive or tape that must be
used in the study
15. Currently treated with GLP-1 analogue, thiazolidinedione (TZD), sulfonylurea,
pramlintide, or SGLT-2 inhibitor medication (use more than 3 months prior to
enrollment is acceptable)
a. If using metformin, participants: i. Must be on a stable dose for 1 month prior to
enrollment ii. Metformin can be continued while the iLet is used
16. Pregnant (positive urine HCG), breast feeding, plan to become pregnant in the next 6
months, or premenopausal participants who are sexually active without use of
contraception
17. Renal failure on dialysis or chronic renal disease with a GFR or eGFR <30mL/min
(values within the last two years will be accepted; if none available or >2 years
prior, participant will be instructed to obtain GFR or eGFR through their usual care
provider and to make copy of result available to study team)
18. Any condition that, in the opinion of the site principal investigator, could interfere
with the safe or effective completion of the study.
a. Conditions to be considered by the investigator may include, but are not limited
to, the following: i. Alcohol or drug abuse ii. Use of prescription drugs that may
dull the sensorium, reduce sensitivity to symptoms of hypoglycemia, or hinder decision
making during the period of participation in the study iii. Coronary artery disease
that is not stable with medical management, including unstable angina, angina that
prevents moderate exercise (e.g. exercise of intensity up to 6 METS) despite medical
management, or within the last 12 months before screening, a history of myocardial
infarction, percutaneous coronary intervention, enzymatic lysis of a presumed coronary
occlusion, or coronary artery bypass grafting iv. Known history of prolonged QTc
interval, malignant arrhythmia, or congenital heart disease v. Congestive heart
failure with New York Heart Association (NYHA) Functional Classification III or IV vi.
History of TIA or stroke in the last 12 months vii. Untreated or inadequately treated
mental illness viii. History of eating disorder within the last 2 years, such as
anorexia, bulimia, or diabulimia or omission of insulin to manipulate weight ix.
History of intentional, inappropriate administration of insulin leading to severe
hypoglycemia requiring treatment
19. Employed by, or having immediate family members employed by Beta Bionics, or being
directly involved in conducting the clinical trial, or having a direct supervisor at
place of employment who is also directly involved in conducting the clinical trial (as
a study investigator, coordinator, etc.); or having a first-degree relative who is
directly involved in conducting the clinical trial
20. Unable to avoid hydroxyurea for duration of study (interferes with accuracy of Dexcom
G6 CGM)
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