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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
- Kanchan Bhasin, MBBS · Phone: (317)-278-2752
Official record on ClinicalTrials.gov — NCT07676565
Locations in the U.S.
| California | Hoag Memorial Hospital, Newport Beach |
| Georgia | Emory University, Atlanta |
| Illinois | Northwestern University, Chicago |
| Maine | Maine Health Research Institute, Portland |
| Massachusetts | Harvard Medical School, Boston |
| Michigan | Henry Ford Hospital, Detroit |
| New York | Mount 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.