Metformin's Anti-Aging effects may depend on your insulin sensitivity
NCT ID NCT04264897
First seen Jun 27, 2026 · Last updated Jul 02, 2026 · Updated 1 time
Summary
This study looked at whether the diabetes drug metformin can slow aging in people without diabetes. Researchers wanted to see if the drug's effects depend on whether a person is insulin sensitive or insulin resistant. Over 12 weeks, 101 adults aged 40-75 took either metformin or a placebo, and their insulin sensitivity, blood sugar, and muscle cell function were measured. The goal was to understand who might benefit most from metformin as an anti-aging treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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166 people
The number who actually took part.
- Started
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Jul 2020
- Finished
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Mar 2025
- Lead sponsor
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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
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40 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 40-75 years of age (inclusive) * Free of chronic disease * Comprehension of the protocol as indicated by an ability to respond to questions about the study after reading the consent form. * Able to use and be contacted by telephone. * Able to speak, read, and understand English, and complete a questionnaire in English * Independently mobile Exclusion Criteria: * Pregnancy * Heart disease (history, abnormal ECG, abnormal stress ECG) * Cerebrovascular disease (history) * Cancer (history) * Chronic respiratory disease (history, forced expiratory volume at one second/forced vital capacity \[FEV1/FVC\] \< 70, FEV1 \< 80% predicted) * Chronic liver disease (history, alanine transaminase \[ALT\] \> 52 IU/L) * Diabetes (history, HbA1C ≥ 6.5, fasting blood glucose≥126 mg/dl, oral glucose tolerance test \[OGTT\] ≥ 200 mg/dl at 2 hrs) * Impaired kidney function (eGFR ,45 mL/min) * B12 lab values outside of normal range (\<193 or \>982 pg/mL) * Alzheimer's (history) * Chronic kidney disease (history, abnormal blood kidney panel including serum creatinine \> 1.4) * Problems with bleeding, on medication that prolongs bleeding time (if subject cannot safely stop prior to biopsy) * Those on glucose lowering drugs * Those planning to have imaging that requires intravenous contrast dye (within 6 weeks) or are on any of the following medications since they are contraindicated with the use of metformin: Dofetilide, Lamotrigine, Pegvisomant, Somatropin, Trimethoprim, Trospium, Gatifloxacin, Cephalexin, Cimetidine, Dalfampridine * Tobacco use * Allergies to lidocaine or metformin
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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
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University of Oklahoma Health Sciences Center, Oklahoma Shared Clinical and Translational Resources
Oklahoma City, Oklahoma, 73104, United States
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University of Wisconsin-Madison
Madison, Wisconsin, 53705, United States
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