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Pilot Study 3 of Outpatient Control-to-Range: Safety and Efficacy With Day-and-Night In-Home Use (CTR3)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT02137512
Recruitment Status : Completed
First Posted : May 13, 2014
Results First Posted : October 19, 2016
Last Update Posted : October 29, 2018
Sponsor:
Information provided by (Responsible Party):
Jaeb Center for Health Research

Brief Summary:

The purpose of this study is to see if an automated insulin management system ("study system") can safely be used at home to manage blood sugar. The study system includes (1) a CGM that measures glucose levels, (2) a computer program on a smartphone that determines how much insulin is needed and allows the study participant user to control the whole system, and (3) an insulin pump that delivers the insulin. The CGM will be from Dexcom. The pump will be from Roche. The CGM and pump are similar to the devices that are currently available for people to purchase and use. However, the smartphone device, the CGM sensor type used with it, and the overall study system can only be used for research at this time.

The study will be completed by about 24 individuals at 6 centers in the United States and Europe. This study has several phases and will take about 11-14 weeks to complete depending on whether the study participant is a CGM user or not.

At selected sites (based on subject eligibility and availability), approximately 10-20 subjects who exhibit safe and competent use of the system at home will be given the option to continue home use of the system in Day-and-Night Closed-Loop mode for up to 5 months.


Condition or disease Intervention/treatment Phase
Type 1 Diabetes Device: Closed-Loop Control System Device: Sensor-Augmented Pump (SAP) Not Applicable

Detailed Description:

The study phases are as follows:

  • Screening visit to see if you are eligible for the study and to determine how long you will need to use the study CGM (visit 1)
  • Up to 3 weeks using the study CGM (depends on your current CGM use), followed by an office visit (visit 2)
  • 2 weeks using the study insulin pump and study CGM together
  • Full day visit in clinic or hotel for training using the system (visit 3)
  • 1 week using the system without automated insulin delivery or suspension
  • 2-day hotel or clinic visit for closed-loop training (visit 4),
  • 16-19 days using the system in the evening and overnight only followed by an office visit (visit 5)
  • 16-19 days using the system for the full 24 hours
  • Final study clinic visit (visit 6)
  • Option 5 month extension phase of day-and-night closed-loop home use

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 30 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Pilot Study 3 of Outpatient Control-to-Range: Safety and Efficacy With Day-and-Night In-Home Use
Study Start Date : August 2014
Actual Primary Completion Date : November 2015
Actual Study Completion Date : November 2015

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Closed-Loop Control System
Use of an investigational control-to-range automated insulin management (artificial pancreas) system using continuous glucose monitoring (CGM) and subcutaneous insulin pump infusion in individuals with type 1 diabetes in the home environment.
Device: Closed-Loop Control System

This investigational device system included the following components:

  • DiAs - a smart-phone medical platform;
  • Dexcom G4 Platinum CGM system connected to DiAs via CGM receiver and USB-Bluetooth relay hardware;
  • Roche Accu-Chek insulin pump connected to DiAs via wireless Bluetooth;
  • Remote Monitoring Server connected to DiAs via 3G or local Wi-Fi network
  • Modular Closed-Loop Control Algorithm Running on DiAs, which is of Control-to-Range (CTR) class
Other Name: Diabetes Assistant (DiAs)

Active Comparator: Sensor-Augmented Pump (SAP)
Use of a study-assigned commercial continuous glucose monitoring (CGM) system and commercial insulin pump
Device: Sensor-Augmented Pump (SAP)

This commercial device system included the following components:

  • Dexcom G4 Platinum CGM system;
  • Roche Accu-Chek insulin pump




Primary Outcome Measures :
  1. Time Spent <70 mg/dL - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values <70 mg/dl during study Main Phase, night only (23:00 to 07:00)


Secondary Outcome Measures :
  1. Time Spent <70 mg/dL - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values <70 mg/dl during study Main Phase

  2. Time Spent <70 mg/dL - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values <70 mg/dl during study Main Phase, day only (07:00 - 23:00)

  3. Time in Range 70-180 mg/dL - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values in range 70-180 mg/dl during study Main Phase

  4. Time in Range 70-180 mg/dL - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values in range 70-180 mg/dl during study Main Phase, night only (23:00 - 07:00)

  5. Time in Range 70-180 mg/dL - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values in range 70-180 mg/dl during study Main Phase, day only (07:00 - 23:00)

  6. Mean Sensor Glucose - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Mean CGM sensor glucose during study Main Phase

  7. Mean Sensor Glucose - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Mean CGM sensor glucose during study Main Phase, night only (23:00 - 07:00)

  8. Mean Sensor Glucose - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Mean CGM sensor glucose during study Main Phase, day only (07:00 - 23:00)

  9. Glucose Coefficient of Variation - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    CGM Glucose Coefficient of Variation (CV) during study Main Phase

  10. Glucose Coefficient of Variation - Main Phase, Night Only [ Time Frame: 2 weeks ]
    CGM Glucose Coefficient of Variation (CV) during study Main Phase, night only (23:00 - 07:00)

  11. Glucose Coefficient of Variation - Main Phase, Day Only [ Time Frame: 2 weeks ]
    CGM Glucose Coefficient of Variation (CV) during study Main Phase, day only (07:00 - 23:00)

  12. Glucose Standard Deviation - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    CGM Glucose Standard Deviation (SD) during study Main Phase

  13. Glucose Standard Deviation - Main Phase, Night Only [ Time Frame: 2 weeks ]
    CGM Glucose Standard Deviation (SD) during study Main Phase, night only (23:00 - 07:00)

  14. Glucose Standard Deviation - Main Phase, Day Only [ Time Frame: 2 weeks ]
    CGM Glucose Standard Deviation (SD) during study Main Phase, day only (07:00 - 23:00)

  15. Time Spent >180 mg/dL - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values >180 mg/dl during study Main Phase

  16. Time Spent >180 mg/dL - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values >180 mg/dl during study Main Phase, night only (23:00 to 07:00)

  17. Time Spent >180 mg/dL - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values >180 mg/dl during study Main Phase, day only (07:00 - 23:00)

  18. Time Spent <50 mg/dL - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values <50 mg/dl during study Main Phase

  19. Time Spent <50 mg/dL - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values <50 mg/dl during study Main Phase, night only (23:00 to 07:00)

  20. Time Spent <50 mg/dL - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values <50 mg/dl during study Main Phase, day only (07:00 - 23:00)

  21. Time Spent <60 mg/dL - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values <60 mg/dl during study Main Phase

  22. Time Spent <60 mg/dL - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values <60 mg/dl during study Main Phase, night only (23:00 - 07:00)

  23. Time Spent <60 mg/dL - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values <60 mg/dl during study Main Phase, day only (07:00 - 23:00)

  24. LBGI - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Low Blood Glucose Index (LBGI) - Main Phase, Day and Night. The LGBI metric is used to quantify the risk of hypoglycemia. A higher LBGI implies more mild hypoglycemic events or less severe hypoglycemic events.

  25. LBGI - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Low Blood Glucose Index (LBGI) - Main Phase, night only (23:00 - 07:00). The LGBI metric is used to quantify the risk of hypoglycemia. A higher LBGI implies more mild hypoglycemic events or less severe hypoglycemic events.

  26. LBGI - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Low Blood Glucose Index (LBGI) - Main Phase, day only (07:00 - 23:00). The LGBI metric is used to quantify the risk of hypoglycemia. A higher LBGI implies more mild hypoglycemic events or less severe hypoglycemic events.

  27. AOC 70 mg/dL - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Area Over the Curve (AOC) 70 mg/dL - Main Phase, Day and Night. The hypoglycemia AOC is scaled to the number of CGM readings so the time factor cancels out. Technically, the units would be mg/dl, but this might seem unintuitive since it is incremental relative to a threshold. For example, a hypoglycemia AOC of 1 mg/dl can denote a glucose of 60 mg/dl for 10% of the time (10 mg/dl below threshold * 10% = 1 mg/dl) or 65 mg/dl for 20% of the time (5 mg/dl below threshold * 20% = 1 mg/dl). Note that it is based on relative (%) rather than absolute time so there is no time element in the resulting units.

  28. AOC 70 mg/dL - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Area Over the Curve (AOC) 70 mg/dL - Main Phase, night only (23:00 - 07:00). The hypoglycemia AOC is scaled to the number of CGM readings so the time factor cancels out. Technically, the units would be mg/dl, but this might seem unintuitive since it is incremental relative to a threshold. For example, a hypoglycemia AOC of 1 mg/dl can denote a glucose of 60 mg/dl for 10% of the time (10 mg/dl below threshold * 10% = 1 mg/dl) or 65 mg/dl for 20% of the time (5 mg/dl below threshold * 20% = 1 mg/dl). Note that it is based on relative (%) rather than absolute time so there is no time element in the resulting units.

  29. AOC 70 mg/dL - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Area Over the Curve (AOC) 70 mg/dL - Main Phase, day only (07:00 - 23:00). The hypoglycemia AOC is scaled to the number of CGM readings so the time factor cancels out. Technically, the units would be mg/dl, but this might seem unintuitive since it is incremental relative to a threshold. For example, a hypoglycemia AOC of 1 mg/dl can denote a glucose of 60 mg/dl for 10% of the time (10 mg/dl below threshold * 10% = 1 mg/dl) or 65 mg/dl for 20% of the time (5 mg/dl below threshold * 20% = 1 mg/dl). Note that it is based on relative (%) rather than absolute time so there is no time element in the resulting units.

  30. HBGI - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    High Blood Glucose Index (HBGI) - Main Phase, Day and Night. The HBGI metric is used to quantify the risk of hyperglycemia. A higher HBGI implies more mild hyperglycemic events or less severe hyperglycemic events.

  31. HBGI - Main Phase, Night Only [ Time Frame: 2 weeks ]
    High Blood Glucose Index (HBGI) - Main Phase, night only (23:00 - 07:00). The HBGI metric is used to quantify the risk of hyperglycemia. A higher HBGI implies more mild hyperglycemic events or less severe hyperglycemic events.

  32. HBGI - Main Phase, Day Only [ Time Frame: 2 weeks ]
    High Blood Glucose Index (HBGI) - Main Phase, day only (07:00 - 23:00). The HBGI metric is used to quantify the risk of hyperglycemia. A higher HBGI implies more mild hyperglycemic events or less severe hyperglycemic events.

  33. ADRR - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Average Daily Risk Range (ADRR) - Main Phase, Day and Night. ADRR is a metric that categorizes risk for hyper and hypoglycemic events. Low risk is scored 0-19, moderate risk is scored 20-40, and high risk is 40 and above.

  34. AUC 180 mg/dL - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Area Under the Curve (AUC) 180 mg/dL - Main Phase, Day and Night. The hyperglycemic AUC is scaled to the number of CGM readings so the time factor cancels out. Technically, the units would be mg/dl, but this might seem unintuitive since it is incremental relative to a threshold. For example, the hyperglycemic AUC is 28 (mg/dl)*days for Patient A and 56 (mg/dl)*days for Patient B when using 180 as the threshold. But this is artificial because Patient B wore the sensor twice as long. So we similarly scale it relative to the number of readings to reflect a mean rather than a sum. So we say hyperglycemic AUC = 4 mg/dl for both patients. Note that time disappears from the units in the scaled version. It represents the mean value of max(glucose-180, 0).

  35. AUC 180 mg/dL - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Area Under the Curve (AUC) 180 mg/dL - Main Phase, night only (23:00 - 07:00). The hyperglycemic AUC is scaled to the number of CGM readings so the time factor cancels out. Technically, the units would be mg/dl, but this might seem unintuitive since it is incremental relative to a threshold. For example, the hyperglycemic AUC is 28 (mg/dl)*days for Patient A and 56 (mg/dl)*days for Patient B when using 180 as the threshold. But this is artificial because Patient B wore the sensor twice as long. So we similarly scale it relative to the number of readings to reflect a mean rather than a sum. So we say hyperglycemic AUC = 4 mg/dl for both patients. Note that time disappears from the units in the scaled version. It represents the mean value of max(glucose-180, 0).

  36. AUC 180 mg/dL - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Area Under the Curve (AUC) 180 mg/dL - Main Phase, day only (07:00 - 23:00). The hyperglycemic AUC is scaled to the number of CGM readings so the time factor cancels out. Technically, the units would be mg/dl, but this might seem unintuitive since it is incremental relative to a threshold. For example, the hyperglycemic AUC is 28 (mg/dl)*days for Patient A and 56 (mg/dl)*days for Patient B when using 180 as the threshold. But this is artificial because Patient B wore the sensor twice as long. So we similarly scale it relative to the number of readings to reflect a mean rather than a sum. So we say hyperglycemic AUC = 4 mg/dl for both patients. Note that time disappears from the units in the scaled version. It represents the mean value of max(glucose-180, 0).

  37. Time Spent >250 mg/dL - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values >250 mg/dl during study Main Phase

  38. Time Spent >250 mg/dL - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values >250 mg/dl during study Main Phase, night only (23:00 to 07:00)

  39. Time Spent >250 mg/dL - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values >250 mg/dl during study Main Phase, day only (07:00 - 23:00)

  40. Time Spent >300 mg/dL - Main Phase, Day and Night [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values >300 mg/dl during study Main Phase

  41. Time Spent >300 mg/dL - Main Phase, Night Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values >300 mg/dl during study Main Phase, night only (23:00 to 07:00)

  42. Time Spent >300 mg/dL - Main Phase, Day Only [ Time Frame: 2 weeks ]
    Percentage of CGM Measured Glucose Values >300 mg/dl during study Main Phase, day only (07:00 - 23:00)


Other Outcome Measures:
  1. Mean Sensor Glucose - Extension Phase [ Time Frame: 3 months ]
    Mean CGM sensor glucose during Extension Phase

  2. Change in HbA1c - Extension Phase [ Time Frame: 5 months ]
    Comparison of HbA1c collected at baseline and at the end of the 5-month extension phase

  3. Time Spent <3.9 mmol/L (70 mg/dL) - Extension Phase [ Time Frame: 3 months ]
    Percentage of CGM Measured Glucose Values <3.9 mmol/L (70 mg/dL) during study Extension Phase

  4. Time Spent <3.3 mmol/L (60 mg/dL) - Extension Phase [ Time Frame: 3 months ]
    Percentage of CGM Measured Glucose Values <3.3 mmol/L (60 mg/dL) during study Extension Phase

  5. Time Spent <2.8 mmol/L (50 mg/dL) - Extension Phase [ Time Frame: 3 months ]
    Percentage of CGM Measured Glucose Values <2.8 mmol/L (50 mg/dL) during study Extension Phase

  6. Time in Range 3.9-10.0 mmol/L (70-180 mg/dL) - Extension Phase [ Time Frame: 3 months ]
    Percentage of CGM Measured Glucose Values in range 3.9-10.0 mmol/L (70-180 mg/dL)

  7. Time Spent >10.0 mmol/L (180 mg/dL) - Extension Phase [ Time Frame: 3 months ]
    Percentage of CGM Measured Glucose Values >10.0 mmol/L (180 mg/dL) during study Extension Phase

  8. Time Spent >13.9 mmol/L (250 mg/dL) - Extension Phase [ Time Frame: 3 months ]
    Percentage of CGM Measured Glucose Values >13.9 mmol/L (250 mg/dL) during study Extension Phase

  9. Time Spent >16.7 mmol/L (300 mg/dL) - Extension Phase [ Time Frame: 3 months ]
    Percentage of CGM Measured Glucose Values >16.7 mmol/L (300 mg/dL) during study Extension Phase

  10. Episodes of Severe Hypoglycemia Events - Extension Phase [ Time Frame: 5 months ]
    Episodes of severe hypoglycemia events during the 5-month extension phase defined as an event requiring assistance of another person due to altered consciousness to actively administer carbohydrate, glucagon, or other resuscitative actions. This means that the subject was impaired cognitively to the point that he/she was unable to treat him or herself, was unable to verbalize his or her needs, was incoherent, disoriented, and/or combative, or experienced seizure or coma. These episodes may be associated with sufficient neuroglycopenia to induce seizure or coma. If plasma glucose measurements are not available during such an event, neurological recovery attributable to the restoration of plasma glucose to normal is considered sufficient evidence that the event was induced by a low plasma glucose concentration.

  11. Episodes of Diabetic Ketoacidosis (DKA) Events - Extension Phase [ Time Frame: 5 months ]
    Episodes of DKA events that occurred during the 5-month extension phase

  12. Reported Serious Adverse Events - Extension Phase [ Time Frame: 5 months ]
    Reported serious adverse events during the 5-month extension phase



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 69 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. 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.
  2. Age >=18 to <70 years.
  3. HbA1c <10.0%; if HbA1c <6.0% then total daily insulin must be >=0.5 U/kg
  4. 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.
  5. Demonstration of proper mental status and cognition for the study.
  6. Currently using insulin-to-carbohydrate ratio to calculate meal bolus sizes
  7. Hypoglycemia awareness as demonstrated by a Clarke Hypoglycemia Awareness score of 2 or lower
  8. Access to internet and cell phone service at home, and a computer for downloading device data.
  9. Living with significant other or family member committed to participating in all 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.
  10. Commitment to maintaining uninterrupted availability via cell phone and avoiding any overnight travel for the duration of each two-week period using the closed-loop system.
  11. An understanding of and willingness to follow the protocol and sign the informed consent.

Exclusion Criteria:

  1. Admission for diabetic ketoacidosis in the 12 months prior to enrollment.
  2. Severe hypoglycemia resulting in seizure or loss of consciousness in the 12 months prior to enrollment.
  3. History of a seizure disorder (except hypoglycemic seizure), unless written clearance is received from a neurologist.
  4. Coronary artery disease or heart failure, unless written clearance is received from a cardiologist.
  5. History of cardiac arrhythmia (except for benign premature atrial contractions and benign premature ventricular contractions which are permitted)
  6. Cystic fibrosis.
  7. 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); 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); testing required within three months prior to admission for subjects with a goiter, positive antibodies, 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)

7. 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 8. 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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02137512


Locations
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United States, California
Sansum Diabetes Research Institute
Santa Barbara, California, United States, 93105
Stanford University
Stanford, California, United States, 94305
United States, Virginia
University of Virginia
Charlottesville, Virginia, United States, 22908
France
Montpellier University Hospital
Montpellier, France, 34295
Israel
National Center for Childhood Diabetes- Schneider Children's Medical Center
Petah Tikva, Israel, 49202
Italy
University of Padova
Padova, Italy, 93106
Sponsors and Collaborators
Jaeb Center for Health Research
Investigators
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Principal Investigator: Roy Beck, MD, PhD Jaeb Center for Health Research
Study Chair: Boris Kovatchev, PhD University of Virginia

Additional Information:
Publications of Results:
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Responsible Party: Jaeb Center for Health Research
ClinicalTrials.gov Identifier: NCT02137512     History of Changes
Other Study ID Numbers: Pilot 3 Outpatient CTR
First Posted: May 13, 2014    Key Record Dates
Results First Posted: October 19, 2016
Last Update Posted: October 29, 2018
Last Verified: August 2018

Keywords provided by Jaeb Center for Health Research:
Artificial Pancreas

Additional relevant MeSH terms:
Layout table for MeSH terms
Diabetes Mellitus, Type 1
Diabetes Mellitus
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Autoimmune Diseases
Immune System Diseases
Insulin
Insulin, Globin Zinc
Hypoglycemic Agents
Physiological Effects of Drugs