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NCT05214573Completed

Second-line Therapies for Patients With Type 2 Diabetes and Moderate Cardiovascular Disease Risk

Source: ClinicalTrials.gov · Last updated 10 Oct 2025

Brief summary (registry, in English)

We will use the target trial framework for causal inference to conduct this observational retrospective cohort study that uses claims data of adults with type 2 diabetes (T2D) included in the de-identified datasets of OptumLabs Data Warehouse (OLDW) and Medicare fee-for-service. In Aim 1, we will emulate a target trial comparing the effectiveness of glucagon-like peptide-1 receptor agonists (GLP-1RA), sodium-glucose cotransporter 2 inhibitors (SGLT2i), dipeptidyl peptidase-4 inhibitors (DPP-4i), and sulfonylureas (SU) in adults with T2D at moderate risk of cardiovascular disease (CVD) with regard to major adverse cardiovascular events (MACE), expanded MACE, microvascular complications, severe hypoglycemia, and other adverse events. In Aim 2, we will compare these four drug classes in the same population of adults with T2D included in OLDW and Medicare fee-for-service data with respect to a set of composite outcomes identified by a group of patients with T2D as being most important to them. Specifically, in Aim 2A, we will prospectively elicit patient preferences toward various treatment outcomes (e.g., hospitalization, kidney disease) using a participatory ranking exercise, then use these rankings to generate individually weighted composite outcomes. Then, in Aim 2B, we will estimate patient-centered treatment effects of four different second-line T2D medications that reflect the patient's value for each outcome. In Aim 3, we will compare different medications within each of the four therapeutic classes with respect to MACE.

Status (registry)
Completed
Study type
Observational
Enrollment
386301 (actual)
First submitted
26 Jan 2022
Start date
Dec 2021
Primary completion date
Sept 2023
Lead sponsor
Mayo Clinic
NCT number
NCT05214573

What you commit to

  • Study type: Observational
  • Participants enrolled: 386301
  • From Dec 2021 to the primary completion date, Sept 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Fill for any study drug during the baseline period or simultaneous (within 30 days) start of ≥2 study drugs

Other illness

  • Type 1 diabetes
  • Metastatic cancer
  • Cognitive impairment.
  • Terminal or advanced illness.

Other

  • Insulin use
  • High risk of CVD
  • Pregnancy
  • Insulin use.
  • Non-English speaking.
  • Residency in a long-term care setting.

Who the study is looking for

  • ≥ 21 years old.
  • Diagnosis of Type 2 diabetes.
  • Use of ≥ 1 study drug (GLP-1RA, SGLT2i, DPP-4i, SU).

Age in the registry: 21 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mayo Clinic - Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.