Status:
COMPLETED
Sensor-Augmented Insulin Delivery: Insulin Plus Glucagon Versus Insulin Alone
Lead Sponsor:
Legacy Health System
Collaborating Sponsors:
Juvenile Diabetes Research Foundation
Oregon Health and Science University
Conditions:
Type 1 Diabetes
Eligibility:
All Genders
21-65 years
Phase:
PHASE2
Brief Summary
This study aims to test an insulin and glucagon delivery algorithm designed to be used in conjunction with a continuous glucose monitoring system. This combined glucose sensing/hormone delivery approa...
Detailed Description
The objective of the current human study is to compare glycemic control in persons with Type 1 Diabetes using the FMPD Insulin plus Glucagon Delivery Algorithm vs. the FMPD Insulin-Alone Algorithm. Su...
Eligibility Criteria
Inclusion
- Age 21-65, history of Type 1 Diabetes Mellitus for \> 3 months.
- Women:
- For women of childbearing potential, a negative urine pregnancy test is required on the first day of the study prior to sensor insertion AND the subject must agree to use contraception prior to and during the study.
- For menopausal women or those who have undergone surgical sterilization, no pregnancy test or contraception will be required.
- Willingness to attend all clinic visits and participate in two 28-hour studies or one 9-hour study.
- Hemoglobin A1C of 5.0-10%. (Values below 5.0 suggest a severe tendency towards hypoglycemia, and values above 10% suggest severely uncontrolled diabetes with risk for ketoacidosis.)
- Body mass index of 19-35.
Exclusion
- Pregnancy, lactation or refusal to use contraception.
- Use of any investigational drug during the 30 days prior to screening.
- Enrollment or participation in any other research studies 30 days prior to and during the entirety of sensor insertion.
- Current alcohol abuse, substance abuse, or severe mental illness (as judged by the Principal Investigator (PI)).
- Any prior cerebrovascular accident or major permanent neurological damage such as aphasia, hemiparesis, or dementia.
- A history of cerebrovascular disease or cardiovascular disease regardless of the time since occurrence.
- Coronary artery disease (symptomatic or asymptomatic) as manifested by unstable angina, acute coronary syndrome, myocardial infarction or therapeutic coronary procedure (e.g., Percutaneous Transluminal Coronary Angioplasty (PTCA), stent placement, Coronary Artery By-pass Grafting (CABG)) within the prior 6 months.
- Any degree of heart failure (as defined by New York Heart Association)..
- Renal insufficiency (serum creatinine of \> 2.5).
- Current foot or leg ulceration.
- Peripheral arterial disease with uncontrolled claudication.
- Active uncontrolled malignancy except basal cell or squamous cell skin cancers.
- Concurrent illness, other than diabetic mellitus, that is not controlled by a stable therapeutic regimen.
- Hemoglobin A1C of less than 5.0 or greater than 10%.
- A total bilirubin level above 1.5 mg/dl.
- Medications: Oral or parenteral corticosteroids (glucocorticoid therapy) are exclusions; topical corticosteroids are not.
- Any chronic immunosuppressive medication (such as cyclosporine, azathioprine, sirolimus, or tacrolimus).
- Visual impairment that would prevent reading the display of the Medtronic Guardian® Receiver.
- Physical impairment that would prevent using the buttons of the Medtronic Guardian® Receiver.
- Serum Alanine Transaminase (ALT) or Aspartate Transaminase (AST) ≥3x the upper limit of normal.
- Serum albumin level of \< 3.2 g/dl.
- Severe anemia as defined by a hematocrit of \< 28%.
- Severe serum electrolyte abnormality (sodium, potassium, carbon dioxide, chloride).
- Cardiac rhythm disturbance characterized by: 2nd or 3rd degree heart block, bradycardia of less than 50 bpm (exception of bradycardia in an aerobic athlete), tachycardia of greater than 100 bpm, or any arrhythmia judged by the investigator to be exclusionary.
- A history of Human Immunodeficiency Virus (HIV) infection.
- An active hepatitis infection.
- Known allergy to any type of insulin
- Insulin resistance requiring more than 200 units of insulin per day
- Known bleeding disorders or chronic usage of warfarin.
- Any known seizure disorder.
- Past history of pheochromocytoma or a family history of Multiple Endocrine Neoplasia (MEN) 2A, MEN 2B, neurofibromatosis, or von Hippel-Lindau disease.
- Hypoglycemic unawareness or chronic hypoglycemia.
- A severe hypoglycemic event which required hospitalization within the past two years.
- Adrenal insufficiency.
- Insulinoma.
- Use of both acetaminophen and ascorbic acid.
- Impaired mentation or psychiatric diagnoses
- Uncontrolled candidiasis.
- Any known allergy to glucagon.
Key Trial Info
Start Date :
November 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2009
Estimated Enrollment :
14 Patients enrolled
Trial Details
Trial ID
NCT00797823
Start Date
November 1 2008
End Date
September 1 2009
Last Update
October 7 2011
Active Locations (1)
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1
Legacy Research
Portland, Oregon, United States, 97232