One finding · Human trial · 2026
Study title
Efficacy and safety of a novel anhydrous 0.1% retinal and 10% azelaic acid concentrate for blemish-prone skin: an eight-week randomized prospective split-face, vehicle-controlled study
- Kind of evidence
- Human trial 2026 · 23 people · participants aged 16-49 (mean 28), Fitzpatrick I-IV, blemish-prone skin · PMID 42572367
- Measured outcome
- Skin effect
- Year
- 2026
- Who was studied
- 23 participants aged 16-49 (mean 28), Fitzpatrick I-IV, blemish-prone skin
- Sample size
- 23
- Measured outcome
- In an 8-week randomized, vehicle-controlled split-face study of 23 people with blemish-prone skin, an anhydrous 0.1% retinal / 10% azelaic acid concentrate improved the pore parameter by 22.3% versus vehicle (p=0.015) and skin texture by 5.6% versus vehicle (p=0.0016), and reduced surface irregularities by 12.7% versus vehicle (p=0.0053).
- Certainty
- Moderate
- Who was measured
- Pore appearance, skin texture and surface irregularities on the face over 8 weeks.
- Study limits
- The pore improvement versus baseline was borderline (15.9%, p=0.051); the small sample completed 23 participants; the product is a six-ingredient concentrate; 10% azelaic acid is regulated as an OTC drug in some markets.
Where it comes from
- Efficacy and safety of a novel anhydrous 0.1% retinal and 10% azelaic acid concentrate for blemish-prone skin: an eight-week randomized prospective split-face, vehicle-controlled study
Published by International Journal of Cosmetic Science (Gaudicheau C, 2026) · Last checked 2026-11-10
Ingredients it was measured on
Skin concerns studied
Other findings on the same ingredient or concern
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