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Clinical Trials/NCT05098301
NCT05098301CompletedNot Applicable

Data Therapy Collection to Evaluate Performances of an Automated Insulin Titration Algorithm Compared to Standard Method of Titration

University Hospital, Montpellier1 site in 1 country30 target enrollmentStarted: November 30, 2021Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
evaluate the performances of an insulin titration algorithm
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

A data collection of blood glucose values, insulin, meal composition will be performed for a period of two months, to evaluate the performances of an automated insulin titration algorithm

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

evaluate the performances of an insulin titration algorithm

Time Frame: day 1

to evaluate the performances of an insulin titration algorithm to calculate insulin therapy parameters at the same precision of an expert practitioner

Secondary Outcomes

  • measure time-in-range evolution adjustment of insulin therapy parameters(day 1)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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