Early Feasibility Study of Zone-MPC and HMS With DiAs in the Outpatient Setting

Diabetes Mellitus, Type 1 Clinical Trial

Official title:

Early Feasibility Study of a Zone-Model Predictive Control (MPC) Controller and a Health Monitoring System (HMS) With the Diabetes Assistant (DiAS) in the Outpatient Setting

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02463682
• Other study ID #: 99796-JPIN
• Status: Completed
• Phase: N/A
• First received: May 28, 2015
• Last updated: April 7, 2016
• Start date: May 2015
• Est. completion date: October 2015

Study information

• Verified date: April 2016
• Source: William Sansum Diabetes Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This is a feasibility study of an artificial pancreas (AP) system with our previously validated Zone-MPC and Health Monitoring System (HMS) algorithms (ClinicalTraisl.gov: NCT01929798) integrated into the Diabetes Assistant (DiAs) system.

Description:

This is a feasibility study of an artificial pancreas (AP) system with our previously validated Zone-MPC and Health Monitoring System (HMS) algorithms (ClinicalTraisl.gov: NCT01929798) integrated into the Diabetes Assistant (DiAs) system. The system will be evaluated on 2-3 subjects per site (n=6-9 subjects) for 2 weeks at 3 different sites (William Sansum Diabetes Center, University of Virginia, and Mayo Clinic, Rochester, MN). Basal rates will be adjusted in a run-to-run manner by study physicians prior to the closed-loop phase for a maximum of 3 weeks. Subjects will then complete 2 weeks at home use of the Zone-MPC/HMS system using the DIAs platform for a closed-loop feasibility trial. The purpose of this pilot study is to establish that safe day-and-night use of the Zone-MPC/HMS system integrated into the DiAs is achievable in the home environment, to analyze and learn to improve upon the run-to- run optimization process, and to collect efficacy data to inform a future larger study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 9
• Est. completion date: October 2015
• Est. primary completion date: October 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 21 Years to 65 Years

Eligibility

Inclusion Criteria:

• Clinical diagnosis, based on investigator assessment, of type 1 diabetes for at least one year and using insulin for at least 1 year and an insulin pump for at least 6 months

• Willing to wear the study CGM device for the duration of the study

• Age =21 to <65 years

• HbA1c <10.0%; if HbA1c <6.0% then total daily insulin must be =0.5 U/kg

• For females, not currently known to be pregnant If female and sexually active, must agree to use a form of contraception to prevent pregnancy while a participant in the study. A negative urine pregnancy test will be required for all premenopausal women who are not surgically sterile. Subjects who become pregnant will be discontinued from the study.

• Demonstration of proper mental status and cognition for the study

• Currently using insulin-to-carbohydrate ratio to calculate meal bolus sizes

• Hypoglycemia awareness as demonstrated by a Clarke Hypoglycemia Unawareness score of 2 or lower

• Access to internet and cell phone service at home, and a computer for downloading device data

• Availability of care partner committed to participating in training activities, knowledgeable at all times of the participant's location, and being present and available to provide assistance when system is being used at night

• Commitment to maintaining uninterrupted availability via cell phone and avoiding any overnight travel for the duration the period using the closed-loop system

• An understanding of and willingness to follow the protocol and sign the informed consent

Exclusion Criteria:

• Admission for diabetic ketoacidosis in the 12 months prior to enrollment

• Severe hypoglycemia resulting in seizure or loss of consciousness in the 12 months prior to enrollment

• History of a seizure disorder (except hypoglycemic seizure), unless written clearance is received from a neurologist

• Coronary artery disease or heart failure, unless written clearance is received from a cardiologist

• History of cardiac arrhythmia (except for benign premature atrial contractions and benign premature ventricular contractions which are permitted)

• Cystic fibrosis

• A known medical condition that in the judgment of the investigator might interfere with the completion of the protocol such as the following examples:

• Inpatient psychiatric treatment in the past 6 months for either the subject or the subject's primary care giver (i.e., parent or guardian)

• Presence of a known adrenal disorder

• Abnormal liver function test results (Transaminase >2 times the upper limit of normal); testing required for subjects taking medications known to affect liver function or with diseases known to affect liver function

• Abnormal renal function test results (calculated GFR <60 mL/min/1.73m2); testing required for subjects with diabetes duration of greater than 5 years post onset of puberty

• Active gastroparesis

• If on antihypertensive, thyroid, anti-depressant or lipid lowering medication, lack of stability on the medication for the past 2 months prior to enrollment in the study

• Uncontrolled thyroid disease (TSH undetectable or >10 mlU/L); testing required within three months prior to admission for subjects with a goiter or who are on thyroid hormone replacement, and within one year otherwise

• Abuse of alcohol or recreational drugs

• Infectious process not anticipated to resolve prior to study procedures (e.g. meningitis, pneumonia, osteomyelitis)

• A recent injury to body or limb, muscular disorder, use of any medication, any carcinogenic disease, or other significant medical disorder if that injury, medication or disease in the judgment of the investigator will affect the completion of the protocol

• Current use of the following drugs and supplements:

• Acetaminophen

• Any medication being taken to lower blood glucose, such as Pramlintide, Metformin,GLP-1 Analogs such as Liraglutide, and nutraceuticals intended to lower blood glucose

• Beta blockers

• Oral or injectable glucocorticoids

• Any other medication that the investigator believes is a contraindication to the subject's participation

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 1

Intervention

Device:
• CGM and Insulin Pump
Dexcom G4 Platinum CGM with Share AP Receiver Roche Accu-Chek insulin pump
• Closed-Loop Control System
The devices that will be used in the Closed-Loop Control System include the following components: DiAs - a smart-phone medical platform; Dexcom Dexcom G4 Platinum connected to DiAs via Bluetooth CGM receiver; Roche Accu-Chek insulin pump connected to DiAs via wireless Bluetooth; Remote Monitoring Server connected to DiAs via 3G or local Wi-Fi network, and Zone-MPC and HMS algorithms running on DiAs (MPC and HMS)

Locations

Country	Name	City	State
United States	University of Virginia	Charlottesville	Virginia
United States	Mayo Clinic	Rochester	Minnesota
United States	William Sansum Diabetes Center	Santa Barbara	California

Sponsors (5)

Lead Sponsor	Collaborator
William Sansum Diabetes Center	Mayo Clinic, University of California, Santa Barbara, University of Padova, University of Virginia

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and efficacy of the system, as assessed by the composite outcome of time in range for glucose levels of 70-180 mg/dL and time < 70 mg/dL.	The primary endpoint for this pilot study will be to determine the safety and efficacy of the system, as assessed by the composite outcome of time in range for glucose levels of 70-180 mg/dL and time < 70 mg/dL, comparing between sensor-augmented pump use (open loop care) (week 1) to closed-loop care (final week), so as to determine the feasibility of eventual long-term use of the system.	1 Week	Yes
Secondary	Time in range for glucose 80-140 mg/dL	Time in range for glucose 80-140 mg/dL at all times unless described otherwise.	1 Week	Yes
Secondary	Time in range for glucose during the nocturnal period	Time in range for glucose 70-180 mg/dL during the nocturnal period.	1 week	Yes
Secondary	Time in Range Postprandial	Time in range for glucose 70-180 mg/dL postprandial, for 5 hours following all meals	1 Week	Yes
Secondary	Markers of hypo- and hyperglycemia	Markers of hypo- and hyperglycemia.	1 Week	Yes
Secondary	Insulin Doses Given	Change in insulin doses given between the open and closed-loop phases of the study.	1 Week	No
Secondary	Treatments for hypoglycemia	Treatments for hypoglycemia between the open and closed-loop phases of the study.	1 week	Yes
Secondary	Number of alerts given by the HMS to prevent hypoglycemia	Number of alerts given by the HMS to prevent hypoglycemia during closed-Loop control.	2 Weeks	Yes
Secondary	Outside interventions needed	Outside interventions needed to aid with treatment during closed-Loop control.	2 Weeks	Yes
Secondary	Failure analysis of the devices/connectivity issues that may occur.	Failure analysis of the devices/connectivity issues that may occur during closed-Loop control.	2 Weeks	Yes