Skip to content

Type 1 Diabetic Post Prandial Glycemia Evaluation Using an Algorithm

Type 1 Diabetic Post Prandial Glycemia Evaluation Using an Algorithm

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05151770
Acronym
EGHYA
Enrollment
40
Registered
2021-12-09
Start date
2021-12-30
Completion date
2022-12-30
Last updated
2023-03-15

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

Conditions

Type I Diabetes

Keywords

Type I diabetes, Hyperglycemia, Post prandial glycemia, algorithm

Brief summary

The aim of this study is to demonstrate the efficacy of an algorithm to anticipate the post prandial glycemic profile in type I diabetic patient.

Interventions

OTHERMeasure of glycemia levels and comparison to algorithm predictions

The study aims to evaluate the efficacy of a new algorithm in predicting the evolution of glycemia levels after a full meal. Glycemia levels measured during and after a full meal will be compared to the values predicted by the algorithm. Composition of the meals will also be collected.

Sponsors

Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
CollaboratorOTHER
Assistance Publique Hopitaux De Marseille
CollaboratorOTHER
M-DT1
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

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

Inclusion criteria

* Type 1 diabetes * ≥ 18 years old * Hb1Ac\<12%

Exclusion criteria

* Patient without continuous glucose monitoring system * Disease other than diabetes (bulimia, anorexia…) * Dialysis patient * Known history of drug or alcohol abuse * Patient under judicial protection * Person deprived of liberty * Pregnant, parturient or breastfeeding woman * Patient in psychiatric care * Patient admitted to a health or social institution for purposes other than research * Any reasons that might interfere with the evaluation of the study objectives

Design outcomes

Primary

MeasureTime frameDescription
Algorithm efficacy15 daysThe Algorithm efficacy in predicting the risk or absence of risk of hyperglycemia two hours after taking a full meal is evaluated by comparing glycemic values calculated by the algorithm and those obtained using continuous glucose monitoring system measurements.

Secondary

MeasureTime frameDescription
Algorithm efficacy (lower margin of error)15 daysThe Algorithm efficacy in predicting the risk or absence of risk of hyperglycemia two hours after taking a full meal is evaluated by comparing glycemic values calculated by the algorithm and those obtained using continuous glucose monitoring system measurements (the accepted margin of error is reduced by 25 to 50% when compared with primary outcome).
Algorithm efficacy versus meal composition15 daysMeals will be analyzed within different groups according to their respective nutritional index. For each group, algorithm prediction reliability will be determined.
Influence of the age of the patients on algorithm results15 daysThe Algorithm efficacy will be analyzed according to the age of patients
Influence of the BMI on algorithms results15 daysWeight and height of patients will be combined to report BMI in kg/m2. Algorithm efficacy will be analyzed according to the BMI of patients
Influence of the insulin administration on algorithm results15 daysData obtained from patients using insulin pumps will be compared to data obtained from patients using multiple daily insulin injections.

Countries

France

Outcome results

None listed

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