The Real-World Control-IQ Glycemic Control and Quality of Life Study in Type 1 Diabetes in France
Recruiting
Observational Study
Diabetes Mellitus, Type 1
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
6 and older
Sex
Any
Study type
Observational
Participants needed
350 (estimated)
Sponsor
Tandem Diabetes Care, Inc. · Industry
Who this trial is looking for
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This post-market surveillance study is primarily designed to demonstrate the ongoing safety of the Control-IQ system, the ongoing performance of glycemic control and quality of life with Control-IQ system use, and the rate of use of the Control-IQ system. The system will be assessed in all approved populations during the first 12 months of use.
Trial Locations
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Facility
City
State
Country
Status
Eligibility Criteria
Inclusion Criteria:
* Clinician-confirmed type 1 diabetes and for whom the site has initiated the t:slim X2 insulin pump with Control-IQ technology (Control-IQ System) with a Dexcom G6 or G7 CGM sensor.
* Age ≥ 6 years at enrollment.
* Using an insulin approved for use in the pump.
* Ability for pa…
Inclusion Criteria:
* Clinician-confirmed type 1 diabetes and for whom the site has initiated the t:slim X2 insulin pump with Control-IQ technology (Control-IQ System) with a Dexcom G6 or G7 CGM sensor.
* Age ≥ 6 years at enrollment.
* Using an insulin approved for use in the pump.
* Ability for patient or parent/guardian to respond to alerts and alarms, and to provide basic diabetes self-management.
* Reside full-time in mainland France.
* Have an email address and mobile phone number
* Participant or participant's parent/guardian has read and understood the information notice and has agreed to participate in the study. This includes agreeing to :
1. use Control-IQ technology, and to continue use for at least 12 consecutive months after study enrollment.
2. the reuse of their clinical data including HbA1c results, obtained at most 4 months prior to enrollment, and as available according to the standard of care during the next 12 months.
3. complete questionnaires per the study protocol.
Exclusion Criteria:
* A medical or other condition, or medications being taken that, in the investigator's judgement would be a safety concern for participation in the study.
* Patients considered vulnerable under French law.
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