Could a cheap pill fix stiff arteries in insulin resistance?
NCT ID NCT03837626
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether amiloride, a drug that blocks sodium channels, can improve artery stiffness and blood vessel function in people who are overweight and insulin resistant. 137 men and women (pre- and postmenopausal) took either amiloride or a placebo daily for 6 months. The main goal was to see if the drug could reduce a key measure of arterial stiffness, which is a risk factor for heart disease.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Amiloride (a pill that blocks sodium channels in cells)
- What this could lead to
- If successful, this could point toward a simple, low-cost way to reduce artery stiffness and heart disease risk in people with insulin resistance.
- What could go wrong
- This is a small, completed trial. The drug may not show clear benefits, or results may not apply to all groups. Amiloride can affect kidney function and electrolyte balance.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
-
137 people
The number who actually took part.
- Started
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Jul 2019
- Finished
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Apr 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
30 to 70 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 30 to 70 years of age at randomization * Body mass index (BMI) 25.1-50 kg/m2 or waist circumference \> 88 cm (\> 35 in) in women and \>102 cm (\>40 in) in men. 3, 4 * One other characteristic of metabolic syndrome (elevated triglycerides ≥150 mg/dl; HDL cholesterol \<40 mg/dl in men and \<50 mg/dl in women; blood pressure ≥130/85 mm Hg or treatment for hypertension; impaired fasting glucose (≥100 mg/dl)) or fasting insulin level \>10 mU/L (correlates with insulin resistance). Exclusion Criteria: 1. History of type 1 or type 2 diabetes 2. Known cardiovascular events within the last 12 months (stroke, acute coronary event, revascularization, heart failure hospitalization). 3. History of uncontrolled thyroid disease, chronic liver disease (cirrhosis) or GFR \<50 ml/min. 4. Use of potassium sparing medications (angiotensin II receptor blockers, angiotensin converting enzymes inhibitors or mineralocorticoid receptor blockers) or use of potassium supplements. 5. Active cancer (This criterion does not apply to those subjects with basal cell carcinoma or stage 1 squamous cell carcinoma of the skin) 6. Excessive alcohol consumption (\>14 drinks/week for men, \>7 drinks/week for women) 7. Current tobacco use 8. Non controlled hypertension 9. Participation in regular exercise \> 3 days/wk per week at a moderate or vigorous intensity 10. Pregnancy or lactation in women (or women not using contraceptives) 11. Women who plan to become pregnant during the duration of the trial 12. Chronic use of NSAIDs 13. Potassium level \> 5.0 mqE/L at time of screening 14. Blood pressure at screening \<110/70
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Missouri Hospital and Clinics
Columbia, Missouri, 65201, United States
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