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Clinical Trials/NCT05282264
NCT05282264CompletedNot Applicable

Acceptability of Hybrid Closed-loop Systems in Patients Living With Highly Unbalanced Type 1 Diabetes

Centre Hospitalier Sud Francilien4 sites in 1 country66 target enrollmentStarted: April 1, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
66
Locations
4
Primary Endpoint
Acceptability of hybrid closed-loop systems

Study Overview

Brief Summary

While closed-loop insulin delivery (CLID) systems demonstrated safety and effectiveness in patients with unbalanced type 1 diabetes (T1D), no studies have included patients with highly and chronically unbalanced diabetes.

The investigators conduct a retrospective, observational, and single-center study to evaluate the acceptability, safety, and efficacy of a CLID system in patients living with T1D (≥2 years) with a HbA1c>11% in the past 12 months and a mean HbA1c >10% over the past three years. Efficacy was assessed using continuous glucose monitoring parameters.

Detailed Description

If hybrid closed-loop systems (HCLS) ("artificial pancreas") for automated insulin administration have demonstrated their great interest in patients living with moderately unbalanced type 1 diabetes (T1D) (HbA1c < 8 .6% on average), no study has looked at their safety, acceptability and efficacy in patients living with highly and chronically unbalanced T1D (HbA1c > 11%). These patients, often young, present more or less advanced microangiopathic complications (retinopathy, nephropathy, neuropathy, etc.) or are highly exposed to the appearance of these complications, the prevention of which, whether primary or secondary, involves obtaining a good glycemic balance over time. These patients "escape" the possibilities of current insulin therapy, whether by multiple insulin injections or by insulin pump, more or less coupled to a continuous glucose monitoring system. Automated insulin delivery systems could be a solution to achieve less catastrophic glycemic control in some of these patients. The investigators are proposing a pilot study aimed at evaluating acceptability, safety and effectiveness of a HCLS currently available in France (the SMARTGUARD™ MINIMED™ 780G or the Control-IQ) in patients followed in the diabetology department of the Centre Hospitalier Sud-Francilien (CHSF), living with highly unbalanced T1D (HbA1c > 11%) in the context of usual follow-up.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients with closed loop system :
  • Adult patients
  • With T1D for at least 2 years
  • Follow-up in the diabetes department of the CHSF
  • Having a laboratory HbA1c > 11% at least once during the past year and at least one other HbA1c > 10% in the previous 3 years
  • Accepting the closed loop system as part of their support
  • Subject informed of the study and not objecting to it
  • Patients without closed loop system :
  • Adult patients
  • With T1D for at least 2 years
  • Follow-up in the diabetes department of the CHSF
  • Having a laboratory HbA1c > 11% at least once during the past year and at least one other HbA1c > 10% in the previous 3 years
  • Refusing the closed loop system as part of their support or
  • Patients for whom a multi-professional medical and paramedical collegial discussion (including diabetologist and nurse referents of the patient) within the service leads to the evaluation of an unfavorable benefit/risk ratio
  • Subject informed of the study and not objecting to it

Exclusion Criteria

  • Patients with closed loop system :
  • Patients without an Internet connection, or without a smartphone or computer
  • Patients for whom a multi-professional medical and paramedical collegial discussion (including diabetologist and patient referent nurse) within the department results in the assessment of an unfavorable benefit/risk ratio (patients with a history of interrupted pump treatment on medical decision, serious psychiatric disorders…)

Outcomes

Primary Outcomes

Acceptability of hybrid closed-loop systems

Time Frame: at 12 months

Maintenance rate of a hybrid closed-loop system in patients living with highly unbalanced T1D (HbA1c \> 11%) and followed in the diabetes department of the CHSF

Secondary Outcomes

  • HbA1c(at day 0)
  • Demographic characteristics : duration of diabete(at day 0)
  • Quality(At baseline, 3, 6, and 12 months)
  • Demographic characteristics : level of education(at day 0)
  • Demographic characteristics : currrent activity(at day 0)
  • Demographic characteristics : age(at day 0)
  • Demographic characteristics : gender(at day 0)
  • Patient satisfaction(At baseline, 3, 6, and 12 months)
  • Hypoglycemia Fear(At baseline, 3, 6, and 12 months)
  • Efficiency(At baseline, 3, 6, and 12 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (4)

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