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Diabeloop for Highly Unstable Type 1 Diabetes (DBLHU)

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. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04042207
Recruitment Status : Recruiting
First Posted : August 1, 2019
Last Update Posted : November 1, 2019
Sponsor:
Information provided by (Responsible Party):
Centre d’Etudes et de Recherche pour l’Intensification du Traitement du Diabète

Brief Summary:

Feasibility study, comparing experimental treatment (DBLHU closed-loop system) with reference treatment (Low Glucose Predictive Suspend system) in 7 patients going through a series of N-of-1 trials. Each N-of-1 trial consists in a prospectively planned, multiple crossover study in a single individual. Two blocks of two periods of four weeks each (closed loop or open loop) will be conducted. Within each block, the sequence closed loop-open loop or open loop-close loop is randomized. Outcomes will be analyzed on the third and fourth weeks of period.

A remote monitoring system managed by specialized nurse on behalf of diabetologist, is provided in closed-loop session.


Condition or disease Intervention/treatment Phase
Diabetes Mellitus, Type 1 Diabetes Mellitus, Brittle Closed-Loop Device: External Insulin Pump Device: Continuous Glucose Monitoring Device: DBLHU System Device: predictive low glucose management technology Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 7 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Intervention Model Description: N-of-1 trials consists in a prospectively planned, multiple crossover study in a single individual.
Masking: None (Open Label)
Primary Purpose: Device Feasibility
Official Title: In Adults With Very Unstable Type 1 Diabetes, is the DBLHU Closed-Loop Insulin Delivery System Able to Improve Blood Glycemic Control Compared to Low-Glucose-Predictive-Suspend System: Two-center, Randomized, Open-label Study
Actual Study Start Date : September 3, 2019
Estimated Primary Completion Date : March 2020
Estimated Study Completion Date : March 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Diabetes Type 1
Drug Information available for: Insulin

Arm Intervention/treatment
Active Comparator: Reference treatment (Open-Loop)
Sensor-augmented pump therapy (SAP) namely the Low Glucose Predictive Suspend system or LGPS and a blinded glucose sensor (Dexcom G6)
Device: External Insulin Pump
Insulin delivery

Device: Continuous Glucose Monitoring
Collection of glucose data

Device: predictive low glucose management technology
This technology allows for the automatic suspension of insulin delivery using a predictive low glucose management algorithm.

Experimental: DBLHU system (Closed-Loop)
DBLHU software (a Model Predictive Control [MPC]-based glucose control algorithm) running on handset associated with the six-generation glucose sensor (Dexcom G6) and Kaleido insulin pump.
Device: External Insulin Pump
Insulin delivery

Device: Continuous Glucose Monitoring
Collection of glucose data

Device: DBLHU System
DBLHU system embeds a regulation algorithm to automatically regulate the patient's glycaemia. It takes as input glycaemia value received every 5 minutes from the CGM and patient inputs related to meals and physical activities and it calculates the amount of insulin to be delivered. It sends this information to the pump that automatically delivers this quantity.




Primary Outcome Measures :
  1. Percentage of CGM time in glucose range 70-180 mg/dl, during 24 hours periods for the third and fourth week for each treatment period [ Time Frame: 14 days for each treatment period ]
    Measured by continuous glucose monitoring


Secondary Outcome Measures :
  1. Evolution over time of the DBLHU system's performance on a day-to-day and determination of the optimization delay of glycemic control [ Time Frame: Over twenty-four hour periods on the four weeks of each treatment period ]
    Measured by continuous glucose monitoring

  2. Percent of CGM time in glucose range 70-180 mg/dl during nighttime. [ Time Frame: Overnight (defined as 23:00 to 07:00) periods on the third and fourth week of each treatment period ]
    Measured by continuous glucose monitoring

  3. Percent of CGM time in glucose range 70-180 mg/dl during daytime. [ Time Frame: Over daytime (defined as 07:00 to 23:00) periods on the third and fourth week of each treatment period ]
    Measured by continuous glucose monitoring

  4. Percent of CGM time with glucose < 70mg/dl, < 60mg/dl and < 50mg/dl [ Time Frame: Over twenty-four hour periods on the third and fourth weeks of each treatment period ]
    Measured by continuous glucose monitoring

  5. Percent of CGM time with glucose > 180mg/dl, 250mg/dl and 300mg/dl [ Time Frame: Over twenty-four hour periods on the third and fourth weeks of each treatment period ]
    Measured by continuous glucose monitoring

  6. Glucose coefficient of variation (CV) and Standard deviation (SD) [ Time Frame: Over twenty-four hour periods on the third and fourth weeks of each treatment period ]
    Measured by continuous glucose monitoring

  7. Rate of CGM excursions below 54 mg/dl (3.0 mM) for at least 15 min [ Time Frame: Over twenty-four hour periods on the third and fourth weeks of each treatment period ]
    Mean time spent in hypoglycaemia, defined as sensor glucose values of 54 mg/dL (3∙0 mmol/L) or lower for more than 15 min consecutively

  8. Comparison of MAGE index and Low Blood Glucose Index (LBGI) [ Time Frame: Over twenty-four hour periods on the third and fourth weeks of each treatment period ]
    Mean amplitude of glucose excursions and Low Glucose index as measured by continuous glucose monitoring

  9. Number of acute metabolic events (severe hypoglycemia, severe Diabetic Ketoacidosis [DKA]) [ Time Frame: During 4 weeks of each treatment period ]

    Measured by continuous glucose monitoring. Number of severe hypoglycemia is defined as any event requiring third party assistance.

    DKA events. Subjects will be asked to measure blood ketone levels on if their interstitial glucose is above 300 mg/l beyond the usual timeframe following a meal, as part of the safety evaluation for hyperglycemia.


  10. For the use and the acceptance, a satisfaction survey will be done on the daily management of diabetes, the modification of daily life with the system dan the fear of hypoglycemia [ Time Frame: At the end of study - on the four weeks of two closed-loop treatment period ]
    DTSQ satisfaction questionnaire, with scale from 6 to 0 where 0 is the worth and 6 the best outcome.



Information from the National Library of Medicine

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Ages Eligible for Study:   22 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Subject (aged 22 or more) with Type 1 diabetes for at least 5 years and confirmed C peptide negative
  • Treated with continuous subcutaneous insulin infusion (CSII) for ≥ 6 months,
  • Trained to carbohydrate counting/flexible insulin therapy,
  • Subject that had experienced, despite optimal diabetes management and prior to any equipment with Smartguard technology, glucose instability as defined by at least 2 of the following criteria which would have led to eligibility for pancreatic islet transplantation:

    • occurrence of at least 1 severe hypoglycemic episode during the past 12 months (need for third party),
    • occurrence of ketoacidosis (hospitalization in ICU) without explanation
    • Impaired awareness of hypoglycemia (Clark Score ≥ 4; Gold Score > 4)
    • glucose levels: standard deviation > 50% of the arithmetic mean value on glucose meter or > 40 mg/dl on CGM on a 14-day recording
    • glucose levels: MAGE (mean amplitude of glucose excursions) index > 60 mg/dl
    • glucose levels: coefficient of variation (CV) > 36%
  • with persisting extreme glucose variability despite optimal medical care
  • with contra-indication or no agreement to undertake pancreatic islet transplantation or pancreas transplantation.
  • Subject willing to wear the DBLHU system continuously throughout the study

Exclusion Criteria:

  • patient with type 2 diabetes
  • age < 22 years old
  • patient without any social or familial support able to intervene in case of severe hypoglycemic event
  • any permanent and severe condition able to interact with the normal course of the study
  • patient with insulin-resistance defined by insulin requirements > 1.5U/kg/d
  • patient with a daily dose of insulin required greater than 90 units
  • patient receiving a total daily dose of insulin less than 8 U
  • use of any insulin that is not 100 U/mL fast-acting insulin analog
  • patient suffering from a serious illness or a treatment that might significantly impair diabetes physiology, i.e. glucose-insulin interactions, that might interfere with the medical device (for example irregular treatment of steroids)
  • patient having severe problems of uncorrected hearing and/or visual acuity
  • patient who is unable to understand and perform all the instructions provided by Diabeloop SA
  • patient not willing to perform ≥4 finger stick blood glucose measurements daily
  • patients that have frequent exposure to magnetic resonance imaging (MRI), computed tomography (CT) scan, or high-frequency electrical heat (diathermy) treatment.
  • patient who has had a pancreatectomy or who has pancreatic malfunctions
  • patient having severely altered renal function (Creatinine clearance < 30ml/min)
  • patient on dialysis
  • pregnancy or breast-feeding patient, or project of pregnancy during the next 6 months
  • lack of effective contraception in women of childbearing potential
  • all conditions excluding participation to clinical research as defined in France

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): NCT04042207


Locations
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France
Grenoble Alpes University Hospital Recruiting
Grenoble, France, 38700
Contact: Pierre Yves BENHAMOU, Pr    +33 4 76765509    PYBenhamou@chu-grenoble.fr   
Principal Investigator: Pierre Yves BENHAMOU, Pr         
Sub-Investigator: Sandrine LABLANCHE, MD         
Lille University Hospital Recruiting
Lille, France, 59037
Contact: Anne VAMBERGUE, Pr    +33 3 20 44 48 21    anne.vambergue@chru-lille.fr   
Principal Investigator: Anne VAMBERGUE, Pr         
Sub-Investigator: Marie-Christine VANTYGHEM, Pr         
Sub-Investigator: Pierre FONTAINE, Pr         
Sponsors and Collaborators
Centre d’Etudes et de Recherche pour l’Intensification du Traitement du Diabète
Investigators
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Principal Investigator: Pierre Yves BENHAMOU, Pr University Hospital, Grenoble

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Responsible Party: Centre d’Etudes et de Recherche pour l’Intensification du Traitement du Diabète
ClinicalTrials.gov Identifier: NCT04042207    
Other Study ID Numbers: 2019-A01365-52
First Posted: August 1, 2019    Key Record Dates
Last Update Posted: November 1, 2019
Last Verified: October 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Centre d’Etudes et de Recherche pour l’Intensification du Traitement du Diabète:
Artificial pancreas
Very Unstable Type 1 diabetes
Additional relevant MeSH terms:
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Diabetes Mellitus
Diabetes Mellitus, Type 1
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Autoimmune Diseases
Immune System Diseases
Insulin
Insulin, Globin Zinc
Hypoglycemic Agents
Physiological Effects of Drugs