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NCT06745063RecruitingPhase 2

Arterial Destiffening Effects of SGLT2 Inhibition in Veterans With Obesity

Source: ClinicalTrials.gov · Last updated 22 Oct 2026

Brief summary (registry, in English)

The study will assign participants to take either the medication, empagliflozin or a placebo for 12 weeks. The goal of the study is to determine the effects of empagliflozin on arterial health in Veterans with obesity.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
50 (estimated)
First submitted
17 Dec 2024
Start date
30 May 2025
Primary completion date
31 Dec 2028
Lead sponsor
VA Office of Research and Development
Diseases
Obesity
NCT number
NCT06745063

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 50
  • From 30 May 2025 to the primary completion date, 31 Dec 2028
  • 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

  • Use of GLP-1 analogs or SGLT2 inhibitors
  • Use of hormone replacement therapy
  • Use of pharmacological therapy for weight loss
  • Change in anti-hypertensive medication regimen (if in use) during the last 90 days

Other illness

  • Diabetes mellitus
  • Uncontrolled hypertension (\>180/90 millimeters of mercury) or systolic \<100 millimeters of mercury at screening visit
  • Known history of cardiovascular disease: heart failure, ischemic heart disease, peripheral artery disease or stroke
  • Diagnosis of chronic kidney disease
  • Active cancer (excluding basal cell carcinoma or stage 1 squamous cell carcinoma of the skin)
  • History of hypersensitivity to nitrates
  • History of ketoacidosis
  • History of recurrent UTIs or mycotic genital infections

Other

  • Unable to provide consent
  • Excessive alcohol consumption (\>14 drinks/week for men, \>7 drinks/week for women)
  • Body weight changes \>10% within the past 6 months
  • Use of anticoagulants
  • Pregnancy

Who the study is looking for

  • Body mass index (BMI) 30-45 kilograms per square meter (kg/m2)
  • 30-60 years of age at randomization
  • Evidence of arterial stiffening (defined as Carotid femoral PWV\>age-predicted) at screening visit (PMID: 20530030), or presence of Stage I hypertension or higher (PMID: 30354655), or current use of antihypertensive agents

Age in the registry: 30 years to 60 years · 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
Harry S. Truman Memorial, Columbia, MO
Coordinator of this site? Confirm its status
ColumbiaUnited StatesRecruiting

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