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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05418699
Other study ID # 2022/P02/540
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date September 26, 2022
Est. completion date January 31, 2025

Study information

Verified date May 2024
Source Groupe Hospitalier de la Rochelle Ré Aunis
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate, in real life, the effect of closed-loop devices on the improvement of glycemic control in diabetic patients managed in the endocrinology departments of secondary care hospitals.


Description:

In recent years, closed-loop insulin delivery have been developed to deliver real-time glucose-responsive insulin to people with type 1 diabetes. Their use has been validated in clinical trials, but international investigative centers participating in clinical trials are not always representative of secondary care centers, and the patients they manage are also different. The eligibility criteria for participants in clinical trials are more stringent and restrictive than those of the usual patient population of diabetes/endocrinology centers. The socio-demographic characteristics of patients in clinical trials, in particular the ratio of males to females, age or ethnicity, do not necessarily reflect those observed in patients actually using the device.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 439
Est. completion date January 31, 2025
Est. primary completion date September 26, 2023
Accepts healthy volunteers No
Gender All
Age group 7 Years and older
Eligibility Inclusion Criteria: - type I diabetic - with a closed-loop insulin pump Exclusion Criteria: - under legal protection order - patient or legal guardian objecting to the use of the data in the research

Study Design


Related Conditions & MeSH terms


Intervention

Device:
closed-loop insulin pump
Follow up of patients with real-time closed-loop insulin delivery systems

Locations

Country Name City State
France CH Béthune-Beuvry Béthune
France CH Boulogne-sur-Mer Boulogne-sur-Mer
France CH Dax Dax
France CHI Mont de Marsan et du Pays des Sources Mont-de-Marsan
France CH Périgueux Périgueux

Sponsors (1)

Lead Sponsor Collaborator
Groupe Hospitalier de la Rochelle Ré Aunis

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary HbA1c level Hemoglobin A1c is an indicator of your long-term glucose levels. Normal range for the hemoglobin A1c level is between 4% and 5.6% At 3 months
Secondary HbA1c level Hemoglobin A1c is an indicator of your long-term glucose levels. Normal range for the hemoglobin A1c level is between 4% and 5.6% At 6 months
Secondary HbA1c level Hemoglobin A1c is an indicator of your long-term glucose levels. Normal range for the hemoglobin A1c level is between 4% and 5.6% At 12 months
Secondary Time in range Percentage of time spent in the target range between 70 and 180 mg/dL in the last 14 days At 3 months
Secondary Time in range Percentage of time spent in the target range between 70 and 180 mg/dL in the last 14 days At 6 months
Secondary Time in range Percentage of time spent in the target range between 70 and 180 mg/dL in the last 14 days At 12 months
Secondary Time below range Percentage of time with glucose values below 70 mg/dL in the last 14 days At 3 months
Secondary Time below range Percentage of time with glucose values below 70 mg/dL in the last 14 days At 6 months
Secondary Time below range Percentage of time with glucose values below 70 mg/dL in the last 14 days At 12 months
Secondary Time above range Percentage of time with glucose values above 180 mg/dL in the last 14 days At 3 months
Secondary Time above range Percentage of time with glucose values above 180 mg/dL in the last 14 days At 6 months
Secondary Time above range Percentage of time with glucose values above 180 mg/dL in the last 14 days At 12 months
Secondary Coefficient of variation Ratio of the standard deviation divided by the mean glucose and multiplying by 100 (percentage) At 3 months
Secondary Coefficient of variation Ratio of the standard deviation divided by the mean glucose and multiplying by 100 (percentage) At 6 months
Secondary Coefficient of variation Ratio of the standard deviation divided by the mean glucose and multiplying by 100 (percentage) At 12 months
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