N/A
Completed N=23
Three-way, Cross-over Closed-loop Exercise Study
Source: ClinicalTrials.gov NCT02241889 ↗Enrolled (actual)
23
Serious AEs
0.0%
Results posted
May 2017
Primary outcomePrimary: Percent of Time With Sensed Glucose < 70 mg/dl — 0.9; 3.2; 0.3 percentage of time
Summary
Blood glucose control systems that utilize both insulin and glucagon to manage blood sugar are paving the way to revolutionize the management of this disease. The benefit of improved control of blood sugar levels compared to standard insulin pump therapy has already been demonstrated. However, the risk of low blood sugar in type 1 diabetes increases considerably during exercise. The investigators research group has shown that small doses of glucagon can prevent low blood sugar when used in a blood sugar control system in patients with type 1 diabetes. However, as insulin sensitivity changes occur very rapidly during exercise, the ability to recognize the onset of physical activity in order to appropriately adjust the insulin and glucagon delivery is vital to helping prevent exercise-induced hypoglycemia.
The purpose of this study is to test how well a new modified blood sugar control system controls blood sugar during exercise compared to: 1) the current system without modifications and 2) standard insulin pump therapy.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percent of Time With Sensed Glucose < 70 mg/dl |
0.9; 3.2; 0.3 | — |
| PRIMARY Percent of Time With Sensed Glucose Between 70-180 mg/dl |
67.6; 72.5; 67.3 | — |
| SECONDARY Mean of the Mean Sensed Glucose Per Participant |
8.6; 8.0; 8.6 | — |
| SECONDARY Number of Carbohydrate Treatments |
0.33; 0.43; 0.29 | — |
| SECONDARY Percent of Time With Sensed Glucose < 50 mg/dl |
0.001; 0.001; 0.0 | — |
| SECONDARY Percent of Time With Sensed Glucose > 180 mg/dl |
26.9; 16.9; 25.2 | — |
| SECONDARY Number of Events Capillary Blood Glucose (CBG) <70 mg/dl |
0.43; 0.33; 0.24 | — |
| SECONDARY Number of Events With CBG Between 70 - 180 mg/dl |
1.6; 3.1; 3.0 | — |
| SECONDARY Number of Events With CBG <50 mg/dl |
1; 0; 1 | — |
| SECONDARY Percent of Time of CBG>180 mg/dl |
1.1; 0.7; 1.1 | — |
Eligibility Criteria
Inclusion Criteria
- Diagnosis of type 1 diabetes mellitus for at least 1 year.
- Male or female subjects 21 to 45 years of age.
- Physically willing and able to perform 45 min of exercise (as determined by the investigator after reviewing the subjects activity level)
- Current use of an insulin pump.
- Willingness to follow all study procedures, including attending all clinic visits.
- Willingness to sign informed consent and HIPAA documents.
Exclusion Criteria
- Female of childbearing potential who is pregnant or intending to become pregnant or breast-feeding, or is not using adequate contraceptive methods. Acceptable contraception includes birth control pill / patch / vaginal ring, Depo-Provera, Norplant, an IUD, the double barrier method (the woman uses a diaphragm and spermicide and the man uses a condom), or abstinence.
- Any cardiovascular disease, defined as a clinically significant EKG abnormality at the time of screening or any history of: stroke, heart failure, myocardial infarction, angina pectoris, or coronary arterial bypass graft or angioplasty. Diagnosis of 2nd or 3rd degree heart block or any non-physiological arrhythmia judged by the investigator to be exclusionary.
- Renal insufficiency (GFR < 60 ml/min, using the MDRD equation as report by the OHSU laboratory).
- Impaired liver function, defined as AST or ALT ≥2.5 times upper limit of normal, according to OHSU laboratory reference ranges.
- Hematocrit of less than or equal to 34%.
- History of severe hypoglycemia during the past 12 months prior to screening visit or hypoglycemia unawareness as judged by the investigator.
- Adrenal insufficiency.
- Any active infection.
- Known or suspected abuse of alcohol, narcotics, or illicit drugs.
- Seizure disorder.
- Active foot ulceration.
- Severe peripheral arterial disease characterized by ischemic rest pain or severe claudication.
- Major surgical operation within 30 days prior to screening.
- Use of an investigational drug within 30 days prior to screening.
- Chronic usage of any immunosuppressive medication (such as cyclosporine, azathioprine, sirolimus, or tacrolimus).
- Bleeding disorder, treatment with warfarin, or platelet count below 50,000.
- Allergy to aspart insulin.
- Allergy to glucagon.
- Insulin resistance requiring more than 200 units per day.
- Need for uninterrupted treatment of acetaminophen.
- Current administration of oral or parenteral corticosteroids.
- Any life threatening disease, including malignant neoplasms and medical history of malignant neoplasms within the past 5 years prior to screening (except basal and squamous cell skin cancer).
- C peptide level of ≥0.5 ng/ml
- Any concurrent illness, other than diabetes, that is not controlled by a stable therapeutic regimen.
- Beta blockers or non-dihydropyridine calcium channel blockers.
- A positive response to any of the questions from the Physical Activity Readiness Questionnaire.
- Any clinically significant disease or disorder which in the opinion of the Investigator may jeopardize the subject's safety or compliance with the protocol.
Data sourced from ClinicalTrials.gov (NCT02241889). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.