Real-world Canadian Retrospective Study Evaluating Longitudinal Semaglutide Use on Cardio-Kidney-Metabolic Outcomes

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorLMC Diabetes & Endocrinology Ltd.

About this trial

The goal of this study is to better understand the real-world effectiveness of semaglutide use on cardio-kidney-metabolic outcomes among adults with T2D and adults with obesity (without diabetes mellitus). This is a retrospective longitudinal analysis using the LMC Diabetes Registry. The primary outcome of the study is to evaluate the change in HbA1c between baseline to 3 years of follow-up among adults with T2D who initiated semaglutide compared to adults with T2D who initiated other AHAs, including sulfonylurea, dipeptidyl peptidase-4 inhibitors, and sodium-glucose cotransporter-2 inhibitors.

Eligibility criteria

Qualifiers

A clinical diagnosis of T2D ≥ 1 year

HbA1c ≥ 6.5% (pre-index date)

Initiated semaglutide or other AHA(s) before January 1st, 2023*

Seen by an LMC endocrinologist in the last 18 months as of the query date

Disqualifiers

Clinical diagnosis of type 1 diabetes/latent autoimmune diabetes in adults (LADA)

Clinical diagnosis of T2D (obesity cohort only)

Are pregnant at the time of semaglutide or other AHA initiation or became pregnant during follow-up period

Documented history or family history of medullary thyroid carcinoma

Trial design

Treatments tested in this trial

  • Semaglutide (SEMA)

Treatment groups

400 Participants
are divided into 3 treatment groups

Locations

This trial has no locations