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A Study of t:Slim X2 With Control-IQ Technology (DCLP5)

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: NCT03844789
Recruitment Status : Active, not recruiting
First Posted : February 18, 2019
Last Update Posted : October 3, 2019
Sponsor:
Collaborators:
Tandem Diabetes Care, Inc.
DexCom, Inc.
Jaeb Center for Health Research
Information provided by (Responsible Party):
University of Virginia

Tracking Information
First Submitted Date  ICMJE February 14, 2019
First Posted Date  ICMJE February 18, 2019
Last Update Posted Date October 3, 2019
Actual Study Start Date  ICMJE June 6, 2019
Estimated Primary Completion Date March 1, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: October 1, 2019)
  • Target in range in main study [ Time Frame: 4 months ]
    The primary outcome for the first phase is time in target range 70-180 mg/dL measured by CGM in CLC group vs. SC group
  • Target in range in extension study [ Time Frame: 3 months ]
    The primary outcome for the extension phase is improving time in range 70-180 mg/dL by CGM when SC (control group) transitions to t:slim X2 with Control-IQ compared with the same group during the Main Phase.
Original Primary Outcome Measures  ICMJE
 (submitted: February 14, 2019)
  • Target in range in main study [ Time Frame: 4 months ]
    The primary outcome for the first phase is time in target range 70-180 mg/dL measured by CGM in CLC group vs. SC) group
  • Target in range in extension study [ Time Frame: 3 months ]
    The primary outcome for the extension phase is improving time in range 70-180 mg/dL by CGM when SC (control group) transitions to t:slim X2 with Control-IQ compared with the same group during the Main Phase.
Change History Complete list of historical versions of study NCT03844789 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE
 (submitted: February 14, 2019)
  • CGM-measured % above 180 mg/dL [ Time Frame: 7 months ]
    Percent
  • GM-measured mean glucose [ Time Frame: 7 months ]
    mg/dL
  • HbA1c at 16 weeks [ Time Frame: 7 months ]
    Percent
  • CGM-measured % below 70 mg/dL [ Time Frame: 7 months ]
    Percent
  • CGM-measured % below 54 mg/dL [ Time Frame: 7 months ]
    Percent
Original Secondary Outcome Measures  ICMJE Same as current
Current Other Pre-specified Outcome Measures
 (submitted: October 1, 2019)
  • % in range 70-140 mg/dL [ Time Frame: 7 months ]
    Percent - CGM measured
  • glucose variability measured with the coefficient of variation (CV) [ Time Frame: 7 months ]
    Coefficient of variation- CGM measured
  • glucose variability measured with the standard deviation (DV) [ Time Frame: 7 months ]
    Standard Deviation- CGM measured
  • % <60 mg/dL [ Time Frame: 7 months ]
    Percent- CGM measured
  • low blood glucose index [ Time Frame: 7 months ]
    index- CGM measured
  • hypoglycemia events (defined as at least 15 consecutive minutes <70 mg\dL) [ Time Frame: 7 months ]
    mg/dL- CGM measured
  • %>250 mg/dL [ Time Frame: 7 Months ]
    Percent- CGM measured
  • % >300 mg/dL [ Time Frame: 7 months ]
    Percent- CGM measured
  • high blood glucose index [ Time Frame: 7 months ]
    index- CGM measured
  • HbA1c < 7.0% at 16 weeks [ Time Frame: 16 weeks ]
    Percent - HbA1c
  • HbA1c <7.5% at 16 weeks [ Time Frame: 16 weeks ]
    Percent - HbA1c
  • HbA1c improvement from baseline to 16 weeks >0.5% [ Time Frame: 16 weeks ]
    Percent - HbA1c
  • HbA1c improvement from baseline to 16 weeks >1.0% [ Time Frame: 16 weeks ]
    Percent - HbA1c
  • HbA1c relative improvement from baseline to 16 weeks >10% [ Time Frame: 16 weeks ]
    Percent - HbA1c
  • Percent - HbA1c improvement from baseline to 16 weeks >1.0% or HbA1c <7.0% at 16 weeks [ Time Frame: 16 weeks ]
    Percent - HbA1c
  • Questionnaire - Fear of Hypoglycemia Survey (HFS-II) - total score, 2 subscales and 4 factor scores: 1- Behavior (avoidance and maintain high BG), 2- Worry (helplessness and social consequences) [ Time Frame: 7 months ]
    Questionnaire
  • Questionnaire - Clarke Hypoglycemia Awareness Scores [ Time Frame: 7 Months ]
    Questionnaire
  • Questionnaire - Problem Areas in Diabetes Survey (PAID) [ Time Frame: 7 Months ]
    Questionnaire
  • Questionnaire - INSPIRE survey scores [ Time Frame: 7 months ]
    Questionnaire
  • Questionnaire - PedsQL Diabetes Module - total score and 5 subscales: 1- Diabetes, 2 - Treatment I, 3 - Treament II, 4 - Worry, 5 - Communication [ Time Frame: 7 months ]
    Questionnaire
  • Questionnaire - Pittsburgh Sleep Quality Index (Parent only) [ Time Frame: 7 months ]
    Questionnaire
  • Questionnaire - System Usability Scale (SUS) [ Time Frame: 7 months ]
    Questionnaire
  • Insulin - Total daily insulin (units/kg) [ Time Frame: 7 months ]
    units/kg
  • Insulin - Basal: bolus insulin ratio [ Time Frame: 7 months ]
    bolus insulin ratio
  • Weight and Body Mass Index (BMI) [ Time Frame: 7 months ]
    Weight and BMI
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE A Study of t:Slim X2 With Control-IQ Technology
Official Title  ICMJE The International Diabetes Closed Loop (iDCL) Trial: Clinical Acceptance of the Artificial Pancreas in Pediatrics: A Study of t:Slim X2 With Control-IQ Technology
Brief Summary The purpose of this study is to learn whether an investigational automated insulin delivery system ("study system") for children with type 1 diabetes can safely improve blood glucose (sometimes called blood sugar) control. The system uses continuous glucose monitoring (CGM), an insulin pump, and a software algorithm to automatically give insulin and control blood glucose. This is called a "closed-loop control" system.
Detailed Description After consent is signed, eligibility will be assessed. Eligible participants not currently using an insulin pump and Dexcom CGM with minimum data requirements will initiate a run-in phase of 2-4 weeks that will be customized based on whether the participant is already a pump or CGM user. Participants who skip or successfully complete the run-in will be randomly assigned 3:1 to the use of closed-loop control (CLC group) using t:slim X2 with Control-IQ Technology vs. Standard of Care (SC) for 16 weeks. The Standard of Care (SC) group will be offered to transition to use CLC and the experimental arm will extend their use of CLC for 12 weeks.
Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Other
Condition  ICMJE Type 1 Diabetes Mellitus
Intervention  ICMJE
  • Device: t:slim X2 with Control-IQ Technology & Dexcom G6 CGM
    Eligible participants will be use the t:slim X2 with Control-IQ Technology & Dexcom G6 CGM technology for 16 weeks during the main study. All participants will be provided the option of continue using the t:slim X2 with Control-IQ system in a 12 week Extension Phase. This arm to be uset:slim X2 with Control-IQ Technology & Dexcom G6 CGM
    Other Name: Experimental
  • Device: Standard of Care
    Eligible participants will be use the study Dexcom G6 CGM for 16 weeks during the main study. All participants will be provided the option of using the t:slim X2 with Control-IQ system in a 12 week Extension Phase.
    Other Name: Control
Study Arms  ICMJE
  • Experimental: Closed Loop Control (CLC)
    Eligible participants not currently using an insulin pump and Dexcom G4, G5 or Dexcom G6 CGM with minimum data requirements will initiate a run-in phase of 2 to 4 weeks that will be customized based on whether the participant is already a pump or CGM user. Participants who skip or successfully complete the run-in will be randomly assigned 3:1 to the use of closed-loop control (CLC group) system using Tandem Control-IQ Technology & Dexcom G6 CGM vs Standard of Care (SC) for 4 months. Participants randomized to the closed loop control (CLC) arm will use the t:slim X2 with Control-IQ Technology & Dexcom G6 CGM for 4 months. All participants will be provided the option of continue using the t:slim X2 with Control-IQ system in a 12 week Extension Phase.
    Intervention: Device: t:slim X2 with Control-IQ Technology & Dexcom G6 CGM
  • Active Comparator: Standard of Care (SC)
    Eligible participants not currently using an insulin pump and Dexcom G4, G5 or Dexcom G6 CGM with minimum data requirements will initiate a run-in phase of 2 to 4 weeks that will be customized based on whether the participant is already a pump or CGM user. Participants who skip or successfully complete the run-in will be randomly assigned 3:1 to the use of closed-loop control (CLC group) system using Tandem t:slim X2 with Control-IQ Technology vs Standard of Care (SC) for 4 months. All participants will be provided the option of using t:slim X2 with Control-IQ system in a 12 week Extension Phase.
    Intervention: Device: Standard of Care
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Active, not recruiting
Actual Enrollment  ICMJE
 (submitted: October 1, 2019)
101
Original Estimated Enrollment  ICMJE
 (submitted: February 14, 2019)
150
Estimated Study Completion Date  ICMJE March 1, 2020
Estimated Primary Completion Date March 1, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  1. Clinical diagnosis, based on investigator assessment, of type 1 diabetes for at least one year and using insulin for at least 6 months
  2. Familiarity and use of a carbohydrate ratio for meal boluses.
  3. Age ≥ 6 and ≤ 13 years old
  4. Weight ≥25 kg and ≤140 kg
  5. 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 serum or urine pregnancy test will be required for all females of child-bearing potential. Participants who become pregnant will be discontinued from the study. Also, participants who during the study develop and express the intention to become pregnant within the timespan of the study will be discontinued.
  6. Living with one or more parent/legal guardian knowledgeable about emergency procedures for severe hypoglycemia and able to contact emergency services and study staff.
  7. Willingness to suspend use of any personal closed loop system that they use at home for the duration of the clinical trial once the study CGM is in use
  8. Investigator has confidence that the participant can successfully operate all study devices and is capable of adhering to the protocol
  9. Willingness to switch to lispro (Humalog) or aspart (Novolog) if not using already, and to use no other insulin besides lispro (Humalog) or aspart (Novolog) during the study for participants using to t:slim X2. This includes:

    • Participants randomized to Control IQ
    • Participants on the SC group on MDI treatment that will be provided a Tandem pump to switch to CSII
    • Participates that are already in Continuous Subcutaneous Insulin Infusion (CSII) randomized to SC during the extension phase when transition to Control IQ
  10. Total daily insulin dose (TDD) at least 10 U/day
  11. Willingness not to start any new non-insulin glucose-lowering agent during the course of the trial
  12. Participant and parent(s)/guardian(s) willingness to participate in all training sessions as directed by study staff.

Exclusion Criteria:

  1. Concurrent use of any non-insulin glucose-lowering agent other than metformin (including glucagon-like peptide [GLP-1] agonists, Symlin, dipeptidyl peptidase 4 [DPP-4] inhibitors, sodium-glucose cotransporter-2 (SGLT2) inhibitors, sulfonylureas).
  2. Hemophilia or any other bleeding disorder
  3. A condition, which in the opinion of the investigator or designee, would put the participant or study at risk (specified on the study procedure manual)
  4. Participation in another pharmaceutical or device trial at the time of enrollment or during the study
  5. Employed by, or having immediate family members employed by Tandem Diabetes Care, Inc., or having a direct supervisor at place of employment who is also directly involved in conducting the clinical trial (as a study investigator, coordinator, etc.); or having a first-degree relative who is directly involved in conducting the clinical trial
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 6 Years to 13 Years   (Child)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT03844789
Other Study ID Numbers  ICMJE DCLP5
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: Yes
Device Product Not Approved or Cleared by U.S. FDA: Yes
Pediatric Postmarket Surveillance of a Device Product: No
IPD Sharing Statement  ICMJE
Plan to Share IPD: Yes
Plan Description: Will follow the NIH Data Sharing Policy and Implementation Guidance on sharing research resources for research purposes to qualified individuals within the scientific community.
Supporting Materials: Study Protocol
Supporting Materials: Statistical Analysis Plan (SAP)
Supporting Materials: Informed Consent Form (ICF)
Time Frame: Generally, data will be made available after the primary publications of each study.
Access Criteria:

The Data Sharing Agreements will be formulated by the Steering Committee in collaboration with the NIH Project Scientist Program Official.

In addition, under special arrangements, complete data sets will be provided to industry partners who would use the data for regulatory clearance (PMA - pre-market approval) of the tested artificial pancreas system. This will be done in response to the specific requirements of RFA-DK-14-024 for this project to "…generate data able to satisfy safety and efficacy requirements by regulatory agencies regarding the clinical testing of artificial pancreas device systems" in the target population of people with type 1 diabetes.

Responsible Party University of Virginia
Study Sponsor  ICMJE University of Virginia
Collaborators  ICMJE
  • Tandem Diabetes Care, Inc.
  • DexCom, Inc.
  • Jaeb Center for Health Research
Investigators  ICMJE
Principal Investigator: Melissa J Schoelwer, MD University of Virginia
PRS Account University of Virginia
Verification Date September 2019

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP