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Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using Hybrid Closed Loop System and Control at Home

Not Applicable
Active, not recruiting
Conditions
Type 1 Diabetes
Interventions
Device: 670G and 770G Insulin Pump
Device: Subject's Current Diabetes Therapy
Registration Number
NCT02748018
Lead Sponsor
Medtronic Diabetes
Brief Summary

The purpose of this study is to evaluate the safety and effectiveness of the Hybrid Closed Loop system (HCL) in adult and pediatric patients with type 1 diabetes in the home setting. A diverse population of patients with type 1 diabetes will be studied. The study population will have a large range for duration of diabetes and glycemic control, as measured by glycosylated hemoglobin (A1C). They will be enrolled in the study regardless of their prior diabetes regimen, including using Multiple Daily Injections (MDI), Continuous Subcutaneous Insulin Infusion (CSII) or Sensor-Augmented Pump therapy (SAP)

Detailed Description

This is a 6 month, multi-center, randomized, parallel, adaptive study in type 1 diabetes with a 6 month continuation period. The study will have three periods, per Cohort:

1. Run-in Period: The run-in period can be up to 60 days during which time a blinded CGM sensor will be worn for two weeks.

2. Study Period: There will be a 6 month randomized study period with two arms: The HCL system and Control.

3. Continuation Period: There will be a 6 month continuation period during which time all subjects will use the HCL system with Auto Mode.

Up to 1500 subjects will be enrolled in order to have 1000 subjects complete the study. Up to 70 investigational Centers in the US, Europe, Canada, Australia and New Zealand will be enrolled.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
280
Inclusion Criteria

Not provided

Exclusion Criteria
  1. Subject participated in any Closed Loop study in the past.
  2. Subject is unable to tolerate tape adhesive in the area of sensor placement
  3. Subject has any unresolved adverse skin condition in the area of sensor placement (e.g., psoriasis, rash, Staphylococcus infection) or area of infusion set placement
  4. Women of child-bearing potential who have a positive pregnancy test at screening or plan to become pregnant during the course of the study
  5. Subject is being treated for hyperthyroidism at time of screening
  6. Subject has an abnormality (out of reference range) in thyroid-stimulating hormone (TSH) at time of screening visit. TSH is not required for subjects 2-13 years of age.
  7. Subject has taken any oral, injectable, or IV glucocorticoids within 8 weeks from time of screening visit, or plans to take any oral, injectable, or IV glucocorticoids during the course of the study.
  8. Subject is actively participating in an investigational study (drug or device) wherein he/she has received treatment from an investigational study drug or investigational study device in the last 2 weeks
  9. Subject is currently abusing illicit drugs or marijuana
  10. Subject is currently abusing prescription drugs
  11. Subject is currently abusing alcohol
  12. Subject is using pramlintide (Symlin), SGLT2 inhibitors, GLP agonists, biguanides, DPP-4 inhibitors or sulfonylureas at time of screening
  13. Subject is using hydroxyurea at the time of screening or plans to use it during the study
  14. Subject has a history of visual impairment which would not allow subject to participate in the study and perform all study procedures safely, as determined by the investigator
  15. Subject has a sickle cell disease, hemoglobinopathy; or has received red blood cell transfusion or erythropoietin within 3 months prior to time of screening
  16. Subject plans to receive red blood cell transfusion or erythropoietin over the course of study participation
  17. Subject diagnosed with current moderate to severe eating disorder such as anorexia or bulimia
  18. Subject has been diagnosed with chronic kidney disease requiring dialysis or resulting in chronic anemia
  19. Subjects who are currently being actively treated for cancer.
  20. Subject who is designated as a research staff member for this study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Hybrid Closed Loop Arm670G and 770G Insulin PumpThe HCL Arm will use the MiniMed System (i.e., using Auto Mode) for 6 months during the study period.
Control ArmSubject's Current Diabetes TherapyThe Control Arm will use individual subject's current diabetes therapy: CSII (Continuous Subcutaneous Insulin Infusion), MDI (Multiple Daily Injections) or SAP (Sensor Augmented Pump). Each cohort (CSII, MDI, or SAP) will be used as the control arm to be compared to the experimental arm (HCL).
Primary Outcome Measures
NameTimeMethod
SAP Cohort: change of A1C (∆A1C) for subjects with baseline A1c > 8%6 months

SAP Cohort: Change in A1C from baseline to the end of the six-month treatment period, defined as A1C measured at the six-month treatment visit minus A1C measured at the randomization visit. This is only for subjects with baseline A1c \> 8%

CSII Cohort: Time in Hypoglycemic Range for subjects with baseline A1c ≤ 8%6 months

CSII Cohort: Time with sensor glucose (SG) below 70 mg/dL (3.9mmol/L) during the six-month study period. This is only for subjects with baseline A1c ≤ 8%

MDI Cohort: Time in Hypoglycemic Range for subjects with baseline A1c ≤ 8%6 months

MDI Cohort: Time with sensor glucose (SG) below 70 mg/dL (3.9mmol/L) during the six-month study period. This is only for subjects with baseline A1c ≤ 8%

CSII Cohort: change of A1C (∆A1C) for subjects with baseline A1c > 8%6 months

CSII Cohort: Change in A1C from baseline to the end of the six-month treatment period, defined as A1C measured at the six-month treatment visit minus A1C measured at the randomization visit. This is only for subjects with baseline A1c \> 8%

MDI Cohort: change of A1C (∆A1C) for subjects with baseline A1c > 8%6 months

MDI Cohort: Change in A1C from baseline to the end of the six-month treatment period, defined as A1C measured at the six-month treatment visit minus A1C measured at the randomization visit. This is only for subjects with baseline A1c \> 8%

SAP Cohort: Time in Hypoglycemic Range for subjects with baseline A1c ≤ 8%6 months

SAP Cohort: Time with sensor glucose (SG) below 70 mg/dL (3.9mmol/L) during the six-month study period. This is only for subjects with baseline A1c ≤ 8%

Secondary Outcome Measures
NameTimeMethod
SAP Cohort: Time in Target Range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Day and Night for all subjects6 months

SAP Cohort: Time in target range measures the time with SG in target range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Day and Night for all subjects

CSII Cohort: Time in Hypoglycemic Range during Night for all subjects6 months

CSII Cohort: Time with SG below 70 mg/dL (3.9mmol/L) during Night for all subjects

CSII Cohort: Time in Hypoglycemic Range for subjects with baseline A1c > 8%6 months

CSII Cohort: Time with sensor glucose (SG) below 70 mg/dL (3.9mmol/L) during the six-month study period. This is only for subjects with baseline A1c \> 8%

MDI Cohort: Time in Hypoglycemic Range for subjects with baseline A1c > 8%6 months

MDI Cohort: Time with sensor glucose (SG) below 70 mg/dL (3.9mmol/L) during the six-month study period. This is only for subjects with baseline A1c \> 8%

MDI Cohort: Change in A1C (∆A1C) for subjects with baseline A1c ≤ 8%6 months

MDI Cohort: Change in A1C from baseline to the end of the six-month treatment period, defined as A1C measured at the six-month treatment visit minus A1C measured at the randomization visit. This is only for subjects with baseline A1c ≤ 8%

SAP Cohort: Time in Hypoglycemic Range for subjects with baseline A1c > 8%6 months

SAP Cohort: Time with sensor glucose (SG) below 70 mg/dL (3.9mmol/L) during the six-month study period. This is only for subjects with baseline A1c \> 8%

SAP Cohort: Time in Target Range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Night for all subjects6 months

SAP Cohort: Time in target range measures the time with SG in target range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Night for all subjects

SAP Cohort: Change in A1C for all subjects6 months

SAP Cohort: Change in A1C from baseline to the end of the six-month treatment period, defined as A1C measured at the six-month treatment visit minus A1C measured at the randomization visit for all subjects

CSII Cohort: Change in A1C (∆A1C) for subjects with baseline A1c ≤ 8%6 months

CSII Cohort: Change in A1C from baseline to the end of the six-month treatment period, defined as A1C measured at the six-month treatment visit minus A1C measured at the randomization visit. This is only for subjects with baseline A1c ≤ 8%

CSII Cohort: Time in Target Range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Night for all subjects6 months

CSII Cohort: Time in target range measures the time with SG in target range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Night for all subjects

SAP Cohort: Change in A1C (∆A1C) for subjects with baseline A1c ≤ 8%6 months

SAP Cohort: Change in A1C from baseline to the end of the six-month treatment period, defined as A1C measured at the six-month treatment visit minus A1C measured at the randomization visit. This is only for subjects with baseline A1c ≤ 8%

SAP Cohort: Time in Hypoglycemic Range during Day and Night for all subjects6 months

SAP Cohort: Time with SG below 70 mg/dL (3.9mmol/L) during Day and Night for all subjects

CSII Cohort: Time in Hypoglycemic Range during Day and Night for all subjects6 months

CSII Cohort: Time with SG below 70 mg/dL (3.9mmol/L) during Day and Night for all subjects

MDI Cohort: Time in Target Range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Night for all subjects6 months

MDI Cohort: Time in target range measures the time with SG in target range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Night for all subjects

MDI Cohort: Time in Hypoglycemic Range during Day and Night for all subjects6 months

MDI Cohort: Time with SG below 70 mg/dL (3.9mmol/L) during Day and Night for all subjects

SAP Cohort: Time in Hypoglycemic Range during Night for all subjects6 months

SAP Cohort: Time with SG below 70 mg/dL (3.9mmol/L) during Night for all subjects

CSII Cohort: Time in Target Range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Day and Night for all subjects6 months

CSII Cohort: Time in target range measures the time with SG in target range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Day and Night for all subjects

CSII Cohort: Change in A1C for all subjects6 months

CSII Cohort: Change in A1C from baseline to the end of the six-month treatment period, defined as A1C measured at the six-month treatment visit minus A1C measured at the randomization visit for all subjects

MDI Cohort: Time in Hypoglycemic Range during Night for all subjects6 months

MDI Cohort: Time with SG below 70 mg/dL (3.9mmol/L) during Night for all subjects

MDI Cohort: Change in A1C for all subjects6 months

MDI Cohort: Change in A1C from baseline to the end of the six-month treatment period, defined as A1C measured at the six-month treatment visit minus A1C measured at the randomization visit for all subjects

MDI Cohort: Time in Target Range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Day and Night for all subjects6 months

MDI Cohort: Time in target range measures the time with SG in target range 70mg/dL (3.9mmol/L) - 180 mg/dL (10.0mmol/L) during Day and Night for all subjects

Trial Locations

Locations (36)

Scripps Health System

🇺🇸

La Jolla, California, United States

University of South Florida Diabetes Center

🇺🇸

Tampa, Florida, United States

Indiana University Health Riley Hospital for Children

🇺🇸

Indianapolis, Indiana, United States

Washington University St. Louis

🇺🇸

Saint Louis, Missouri, United States

SUNY Upstate Medical University

🇺🇸

Syracuse, New York, United States

Stanford University

🇺🇸

Palo Alto, California, United States

Atlanta Diabetes Associates

🇺🇸

Atlanta, Georgia, United States

University of Michigan

🇺🇸

Ann Arbor, Michigan, United States

Sanford Health

🇺🇸

Sioux Falls, South Dakota, United States

Rainier Clinical Research

🇺🇸

Renton, Washington, United States

A.S.S.T. Spedali Civili

🇮🇹

Brescia, Italy

Hospital Universitario Virgen del Rocío

🇪🇸

Sevilla, Spain

Center of Excellence in Diabetes & Endocrinology

🇺🇸

Sacramento, California, United States

Sansum Diabetes Research Institute

🇺🇸

Santa Barbara, California, United States

Barbara Davis Center

🇺🇸

Aurora, Colorado, United States

Initernational Diabetes Center

🇺🇸

Minneapolis, Minnesota, United States

International Diabetes Center

🇺🇸

Minneapolis, Minnesota, United States

SoCal Diabetes

🇺🇸

Torrance, California, United States

Endocrine Research Solutions

🇺🇸

Roswell, Georgia, United States

Rocky Mountain Diabetes

🇺🇸

Idaho Falls, Idaho, United States

Grunberger Diabetes Institute

🇺🇸

Bloomfield Hills, Michigan, United States

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

Texas Diabetes & Endocrinology

🇺🇸

Austin, Texas, United States

University of Washington

🇺🇸

Seattle, Washington, United States

Westminster Endocrine & Diabetes Research Society

🇨🇦

New Westminster, British Columbia, Canada

Diabeteszentrum für Kinder und Jugendliche, Kinder- und Jugendkrankenhaus Auf der Bult

🇩🇪

Hannover, Germany

Diablo Clinical Research

🇺🇸

Walnut Creek, California, United States

IDERC

🇺🇸

Des Moines, Iowa, United States

Diabetes and Glandular Disease Clinic, P.A.

🇺🇸

San Antonio, Texas, United States

Hôpital Necker Enfants Malades

🇫🇷

Paris, France

HCL - Lyon Sud

🇫🇷

Pierre-Bénite, France

Dunedin Public Hospital

🇳🇿

Dunedin, New Zealand

Children's Hospital of Eastern Ontario

🇨🇦

Ottawa, Canada

Dept Internal Medicine, Örebro University Hospital

🇸🇪

Örebro, Sweden

Cambridge University Hospitals NHS Foundation Trust - Addenbrooke's Hospital

🇬🇧

Cambridge, United Kingdom

New Zealand Clinical Research

🇳🇿

Christchurch, New Zealand

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