Vitamin B3 cream or pills: which works better to stop skin spots?
NCT ID NCT07049068
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested whether taking nicotinamide (a form of vitamin B3) as a pill or applying it as a cream could reduce precancerous skin spots called actinic keratoses on the face. 74 adults with at least three such spots were randomly assigned to receive either oral nicotinamide plus a placebo cream, or topical nicotinamide plus a placebo pill for 6 months. The goal was to see which method worked better at preventing new spots and shrinking existing ones.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Nicotinamide (a form of vitamin B3)
- What this could lead to
- If it works, this could point toward a simple, affordable way to prevent precancerous skin spots using vitamin B3.
- What could go wrong
- This is a small, early-phase study (Phase 1) with only 74 people. Results may not apply to everyone, and the effect might be small or not better than placebo.
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 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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74 people
The number who actually took part.
- Started
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Feb 2022
- Finished
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Nov 2024
- 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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18 years and older
- 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.
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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: * male individuals over 18 years of age * female individuals with tubal ligation, hysterectomy or over 45 years of age in menopause * presence of at least three palpable actinic keratoses on the face Exclusion Criteria: * individuals with an incidence of 3 or more squamous cell carcinomas in the last year * solid organ transplant recipients * carriers of the human immunodeficiency virus (HIV) * solid organs cancer * active gastric ulcer * recent history of acute myocardial infarction * hypotension * pregnancy * lactation * chronic liver disease * liver or kidney failure * xeroderma pigmentosum * albinism * epidermodysplasia verruciformis * dystrophic epidermolysis bullosa * nevoid basal cell carcinoma syndrome * individuals with a large number of confluent actinic keratosis (making it impossible to count individual lesions) * Individuals using carbamazepine * Individuals using oral retinoids * Individuals using oral supplements containing nicotinamide * Individuals who had undergone field treatments for actinic keratoses such as 5-fluorouracil in the last 4 months * individuals who were unable to understand the objectives and risks of treatment * Individuals who refused to participate or sign the consent form
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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
-
Programa de Pós Graduação Ciencias Médicas UFRGS
Porto Alegre, Rio Grande do Sul, 90035003, Brazil
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