Prediabetes drug study pulled before it began
NCT ID NCT06526494
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study was designed to test whether metformin, a common diabetes drug, could improve blood vessel function in people with prediabetes. It planned to enroll adults aged 18-55 with prediabetes and compare metformin to a placebo over 12 weeks. However, the study was withdrawn before any participants were enrolled, so no results are available.
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
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Started
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Nov 2024
- Finished
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Dec 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
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18 to 55 years
- Sex
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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: * Age 18-55 years * Prediabetes defined as an HbA1c between 5.7% and 6.4% * Able to provide informed consent Exclusion Criteria: * Current use of metformin or metformin use within the past 12 months * Current use of medicated contraindicated for use with metformin * Current use of vitamin C supplement * Current smoker or quit smoking within the last 6 months * Pregnant, breastfeeding, planning to become pregnant, or unwilling to use adequate birth control * Uncontrolled hypertension (Systolic blood pressure \>140 mmHg) * Body Mass Index \> 40 kg/m2 * History of diabetes, myocardial infarction, heart failure, liver disease, or chronic kidney disease (estimated glomerular filtration rate \< 45 ml/min/1.73m2) * History of lactic acidosis * History of alcohol abuse * Severe infection within the last 30 days * Immunosuppressive therapy within the past year * Life expectancy \< 1 year * Allergy to metformin, nitroglycerin, sodium nitroprusside, ringer's lactate * Study compliance: Unwilling to fast overnight, have an intravenous catheter placed, take a study drug for 12 weeks, or visit Iowa campus 6 times within a 12-16 week period
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Genom att skicka in godkänner du våra Användarvillkor
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 Iowa
Iowa City, Iowa, 52242, United States
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University of Iowa Hospitals and Clinics
Iowa City, Iowa, 52245, United States
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