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Safety and Efficacy of Adjunct Therapies in Adults With Type 1 Diabetes: Multicenter, Registry Study

RecruitingObservational study

Safety and Efficacy of Adjunct Therapies in Adults With Type 1diabetes: Multicenter, Registry Study

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Adults ≥18 years of age
* Clinical diagnosis of T1D
* GLP-1RA or SGLTi (SGLT-1 and SGLT-2 inhibitors) drug prescribed by their provider for any indication as part of usual care with use for no more than 1 week
* Use of CGM and availability of CGM data for 1 month prior to enrollment and expected to be available throughout the study
* Willing and able to provide informed consent

Exclusion Criteria:

* No exclusion criteria other than those not meeting inclusion criteria above

About the study

This will be a multicenter registry-based study to evaluate safety and efficacy of GLP-1RA and SGLTi therapies in adjunct to insulin in adults with type 1 diabetes (T1D) over 1 year. This study will enroll participants who have been prescribed adjunct therapy as part of usual care.

Sponsor: Indiana University · Participants: 300 · Started: Mar 24, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07676565

Locations in the U.S.

CaliforniaHoag Memorial Hospital, Newport Beach
GeorgiaEmory University, Atlanta
IllinoisNorthwestern University, Chicago
MaineMaine Health Research Institute, Portland
MassachusettsHarvard Medical School, Boston
MichiganHenry Ford Hospital, Detroit
New YorkMount Sinai, New York

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.