Evaluation of Glycemic Control in Adults With Type 1 Diabetes When Switching to Insulin Degludec

NCT ID: NCT05434559

Last Updated: 2022-12-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

475 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-02-20

Study Completion Date

2022-10-31

Brief Summary

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Retrospective multicenter study analyzing data gathered from medical records and diabetes management platforms to assess the effect of using Insulin Degludec (Tresiba®) on measures of diabetes control.

People with type 1 diabetes who switched to Insulin Degludec from another basal insulin between 1/5/2019 and 1/6/2021 will be included.

Glycemic control from 12 months before the switch to Insulin Degludec will be compared to glycemic control of the 12 months after the switch.

Detailed Description

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Conditions

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Type 1 Diabetes

Keywords

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Insulin Degludec Continuous Glucose Monitoring

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Study cohort

People with type 1 diabetes who switched to Insulin Degludec from another basal insulin between 1/5/2019 and 1/6/2021 in the two participating sensors

Insulin Degludec

Intervention Type DRUG

Switch during standard routine care to Insulin Degludec.

Interventions

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Insulin Degludec

Switch during standard routine care to Insulin Degludec.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* People with T1D ≥18 years at the moment of switch to Insulin Degludec
* Diagnosed with T1D ≥2 years before switch to Insulin Degludec
* On basal-bolus insulin therapy with insulin pens ≥2 years before switch to Insulin Degludec
* ≥6 months use of Insulin Degludec at moment of datacollection
* Using continuous glucose monitoring ≥2 years before switch to Insulin Degludec

Exclusion Criteria

* People with T1D \<18 years at the moment of switch to Insulin Degludec
* People without T1D or with T1D \<2 years before switch to Insulin Degludec
* Women with T1D who are pregnant or planning pregnancy during -12 and +12 months
* Not using basal-bolus insulin therapy with insulin pens during -24 and +6 months
* Start to use non-insulin antidiabetic agents between -12 and +12 months
* Having received treatment with oral or injectable corticosteroids during -12 and +12 months
* Undergoing hemodialysis, renal transplantation, or beta cell transplantation during -12 and +12 months
* \<6 months use of Insulin Degludec at moment of datacollection
* Not using continuous glucose monitoring or \<2 years before switch to Insulin Degludec
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Antwerp

OTHER

Sponsor Role collaborator

prof dr Pieter Gillard

OTHER

Sponsor Role lead

Responsible Party

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prof dr Pieter Gillard

Coordinating Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Universitaire Ziekenhuizen Leuven

Leuven, , Belgium

Site Status

University Hospital Antwerp

Wilrijk, , Belgium

Site Status

Countries

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Belgium

References

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De Groote R, Lefever E, Charleer S, Donne P, De Block C, Mathieu C, Gillard P. Continuous Glucose Monitoring-Derived Glucometrics in Adults with Type 1 Diabetes When Switching Basal Insulins. Diabetes Technol Ther. 2024 Aug;26(8):587-595. doi: 10.1089/dia.2023.0616. Epub 2024 Apr 9.

Reference Type DERIVED
PMID: 38512387 (View on PubMed)

Other Identifiers

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S66239

Identifier Type: -

Identifier Source: org_study_id