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Efficacy and Safety Assessment of Niacinamide Cosmetic Preparation: a Randomized Controlled Trial

Testing the Efficacy and Safety of Niacinamide Cosmetic Preparation: A Randomised, Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06189105
Enrollment
25
Registered
2024-01-03
Start date
2023-06-03
Completion date
2024-06-01
Last updated
2024-01-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dry Skin; Eczema, Skin Hyperpigmentation

Brief summary

Niacinamide in lower concentrations has been recognized as a cosmetic ingredient with hydrating properties. Therefore, aim was to test the efficacy and safety of niacinamide cosmetic preparation in A Randomized, Controlled Trial.

Detailed description

Skin hydration (as use of hydrating cosmetic ingredients) is one of the most interventions for healthy skin and skin barrier function. Therefore, cosmetic ingredients used for this purpose should be examined for their efficacy.

Interventions

OTHERmiss alice face it you love me serum

Facial serum with niacinamide, plant-based collagen and peptides will be applied by each participant to the treatment site according to randomization protocol every evening

OTHERNo treatment (usual skincare rutine)

No treatment (usual skincare rutine)

Sponsors

University of Split, School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* healthy volunteers who gave written informed consent

Exclusion criteria

* skin disease, skin damage on measurement sites, use of corticosteroids and immunomodulators a month prior to the inclusion and during the trial, non-adherence to the trial protocol, exposure to artificial UV radiation, pregnancy and lactation

Design outcomes

Primary

MeasureTime frameDescription
TEWL assessment with Courage Khazaka probethrough study completion, an average of 1 yearTransepidermal water loss
Hydration assessment with corneometer probethrough study completion, an average of 1 yearstratum corneum hydration
pigmentation assessment with mexameter probethrough study completion, an average of 1 yearerythema and melanin
skin oiliness assessment with sebumeter probethrough study completion, an average of 1 yearsebum level

Secondary

MeasureTime frameDescription
subjective opinion of participantsthrough study completion, an average of 1 yearparticipants notes on skin rection

Countries

Croatia

Contacts

Primary ContactJosipa Bukic
jbukic@mefst.hr00385917933752

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026