Chromium picolinate shows promise for teen skin condition linked to insulin resistance
NCT ID NCT07371169
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether taking chromium picolinate daily for 24 weeks could reduce the severity of acanthosis nigricans (dark, thick skin patches) and improve insulin resistance in adolescents aged 12 to 18. Researchers compared the supplement to a placebo in 90 participants. The goal was to see if a simple supplement could help manage these conditions without major side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- chromium picolinate
- What this could lead to
- If it works, this could point toward a simple supplement to help manage skin changes and insulin resistance in teens.
- What could go wrong
- This is a small, completed trial with 90 participants, so results may not apply broadly. Chromium supplements can have side effects and may not be effective for everyone.
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
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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90 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Jan 2026
- 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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12 to 18 years
- Sex
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Anyone
- Healthy volunteers
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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: * Adolescent patients of both sexes, aged 12 to 18 years. * Clinically diagnosed with acanthosis nigricans. * Present Insulin resistance, defined as Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) ≥ 2.5. * Willing to participate in the study, with written informed consent provided by both the patient and guardian. Exclusion Criteria: * Diagnosis of type 1 or type 2 diabetes mellitus. * Known hypersensitivity to chromium or any of the capsule excipients. * Use of insulin-sensitizing medications (e.g., metformin, thiazolidinediones) within 3 months before screening. * Use of systemic corticosteroids or other medications known to affect glucose metabolism within 3 months before screening. * Significant renal disease (estimated glomerular filtration rate \< 60 mL/min/1.73 m²) or liver disease (alanine aminotransferase or aspartate aminotransferase \> 2.5 times the upper limit of normal). * Pregnancy or lactation.
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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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Baghdad Medical City / Children Welfare Teaching Hospital / Department of Endocrinology
Baghdad, Baghdad Governorate, 10045, Iraq
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Other studies related to the condition(s) this trial covers.
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