CI

At a glance

ClinicalIndex Comparison Record
Early Ph 1Completed· 61 enrolled / 61 target
Drug / intervention
Ertugliflozindrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04167761
NCT04167761Early Ph 1CompletedOn Track (0.8/mo)Completion was 30mo ago

Ertugliflozin: Cardioprotective Effects on Epicardial Fat

Stanford University·interventional·Posted Nov 19, 2019·Updated Jun 4, 2026

In Brief

A Early Phase 1 clinical trial evaluating Ertugliflozin for Cardiovascular Diseases and 3 related conditions. Completed, enrolled 61 participants across 1 site.

Detailed Summary

The purpose of this study is to learn if Sodium-Glucose Cotransporter 2 inhibitor (SGLT2i) medications enhance beneficial properties of epicardial adipose tissue including metabolic flexibility, insulin sensitivity, decreased cell size and reduced inflammation.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Early Ph 1CompletedFinished
2020202120222023202420252026
First PostedNov 19, 2019
Enrollment StartJul 1, 2020
Primary CompletionDec 31, 2023
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 6.6 years ago

Arms & Interventions

Ertugliflozin (treated tissue)experimental

Adipose tissue samples collected from participants were treated with Ertugliflozin at a concentration of 25 µM in vitro. Tissue samples were incubated with Ertugliflozin to evaluate its effects on lipolysis, inflammation, and gene expression in epicardial, pericardial, and subcutaneous adipose tissues

Drug: Ertugliflozin

Interventions

Ertugliflozindrug

Adipose tissue samples collected from participants were treated with Ertugliflozin at a concentration of 25 µM in vitro. This treatment was applied in a laboratory setting to assess the effects of Ertugliflozin on lipolysis, inflammatory cytokine release, and gene expression in epicardial, pericardial, and subcutaneous adipose tissue