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Study to Assess the Metabolic Impact of IRTA© and Patients Satisfaction in Type 1 Diabetic Patients, Treated by Either Insulin Pump or Multiple Daily Insulin Injections, and Using Freestyle Libre®, a Real-time Continuous Glucose Monitoring

Clinical Evaluation of Insulin Real-Time Advisor (IRTA©): a Decision Support Software for Insulin Therapy Combined With Freestyle Libre®, a Continuous Glucose Monitoring System: Glycemic Impact and Satisfaction in Type 1 Diabetic Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04211220
Acronym
IRTA
Enrollment
64
Registered
2019-12-26
Start date
2020-01-09
Completion date
2022-03-03
Last updated
2022-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes

Keywords

Real time continuous glucose monitoring, Decision support software

Brief summary

A prospective monocentric before and after study, ruled in 2 periods of 3 months : during the first period, the patient will adjust insulin treatment as usual, during the second period, the patient will adjust insulin treatment with IRTA support

Detailed description

Freestyle Libre® continuous glucose monitoring (CGM) system may improve glycemic control. However, this system contributes to the complexity of insulin adjustment by the diversity of the data delivered by CGM system. Insulin Real-Time Advisor (IRTA©), a decision support software, has been developed in order to guide patients in the adaptation of their treatment according to CGM data. IRTA© provides advice applicable to thousand situations according to six parameters: glucose level, trend arrows, meals, physical activity, before bedtime, time since the previous bolus. Type of advice : * Insulin injection (carb and correction) * To continue treatment without modification * To lower the insulin dose (temporary basal rate) * Sugar intake advice * Glucose level control with CGM, self-monitor blood glucose, blood ketones monitor * To change catheter for patients treated by insulin pump.

Interventions

Insulin pump Continuous glucose monitoring

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

A decision support software

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Men and women ≥ 18 years of age * Patients with type 1 diabetes mellitus for more than 2 years * Treated by either insulin pump for more than 6 months or multiple daily insulin injections. * Using Freestyle Libre® for more than 3 months * Accepting IRTA use * Patient able to provide free and informed consent * Patient able to provide written non-disclosure agreement

Exclusion criteria

* Pregnancy, breastfeeding or pregnancy project in the future 6 months * Patients with no smart phone or internet access * Patients legally protected (under judicial protection, guardianship or supervision) * Patients with acute illness (psychiatric, infection, cancer,…) * Patients using another CGM system (Enlite® or Dexcom G4®)

Design outcomes

Primary

MeasureTime frameDescription
Percentage of time spent in 70-180mg/dl (time in range) in the last month of each period of the study (without and then with IRTA©)6 monthsAssessment of the metabolic impact of IRTA© on time in range (time spent in the standard glucose range between 70-180mg/dl, ie 3.9-10mmol/l) in type 1 diabetic patients, treated by either insulin pump or multiple daily insulin injections, and using Freestyle Libre®.

Secondary

MeasureTime frameDescription
Time spent in glucose level higher than 250 mg/dl6 months
Time spent in glucose level higher than 180 mg/dl6 months
Time spent in glucose level lower than 70 mg/dl6 months
Time spent in glucose level lower than 54 mg/dl6 months
Number of incidents (severe hypoglycemia, diabetic ketoacidosis, hospitalizations related to poor glycemic control)6 months
Percentage of time spent with or without CGM6 months
Comparison of HbA1c level at the end of each period of the study (without / with IRTA©)6 monthsBlood sample at inclusion, 3 months and 6 months
Patients' satisfaction related to CGM and the impact of IRTA© on this satisfaction6 monthsCGM Satisfaction (CGM-SAT) 44-item questionnaire. Higher scores reflect more favorable impact of, and satisfaction with, CGM use.
Patients' satisfaction related to IRTA©6 monthsSatisfaction questionnaire: 5-point Likert scale (1 = strongly agree; 5 = strongly disagree) with each of 18 items.
Number of connections to the IRTA system6 months
Number of advice given by the IRTA system6 months
Type of advice given by the IRTA system that is more often asked6 months
Glycemic variability6 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026