Empagliflozin Reversal of Arterial StiffnEss in Aging
University of Missouri-Columbia · NCT06506422
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 60–80 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 2, Phase 3
- Target enrollment
- 80
- US sites recruiting
- 1
- Study start
- August 18, 2024
- Record last updated
- February 6, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Randomized placebo-controlled clinical trial in a cohort of males (n=40) and females (n=40), 60-80 years of age, with the hypothesis that SGLT2 inhibition with empagliflozin (10mg/day for 12 weeks) reduces aging-related arterial stiffening.
Being studied: Empagliflozin 10 MG; Placebo
Conditions: Aging; Arterial Stiffness
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Able to provide consent
- 60 to 80 years of age at randomization (women must be postmenopausal defined as more than 1 year without menses)
- Stable anti-hypertensive medication regimen (if in use) for at least 90 days
- Evidence of arterial stiffening (defined as carotid-femoral PWV >/= 8 m/s) at the time of screening visit.
Exclusion Criteria
- Diabetes
- BMI>/= 45kg/m2
- Known history of cardiovascular disease: heart failure, ischemic heart disease, peripheral artery disease or stroke
- Estimated glomerular filtration rate GFR \< 29 mL/min
- Active cancer (excluding basal cell carcinoma or stage 1 squamous cell carcinoma of the skin)
- Excessive alcohol consumption (>14 drinks/week for men, >7 drinks/week for women)
- Use of hormone replacement therapy
- Body weight change ≥10% within the last 6 months
- Uncontrolled hypertension during screening visit (>180/110 mmHg)
- Symptomatic hypotension and/or a SBP \<100 mmHg
- History of ketoacidosis
- High fall risk per assessment of study physician and/or safety officer at the time of screening (results must be abnormal for both fall risk assessments and orthostatic blood pressure measurements)
- Anticipated need of prolonged fasting
- History of recurrent UTIs or mycotic genital infections
- Following a low-carbohydrate diet (\<20 grams/day)
- Participation in regular exercise > 3 days/week per week at a moderate or vigorous intensity
- Known sensitivity to nitrate medications
Recruiting US locations
University of Missouri
Columbia, MO 65211
Site contact: Andrea Atkins, BSN · 573-884-1222 · wiesa@health.missouri.edu
Study contacts (from the official record)
- Camila Manrique, MD · (573) 882-2554 · manriquec@health.missouri.edu
- Andrea Atkins, BSN · (573) 884-1222 · wiesa@health.missouri.edu
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