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Normaderm Phytosolution Global Observational Study

Benefit of a Dermocosmetic in Mild to Moderate Adult Acne

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05483205
Enrollment
2827
Registered
2022-08-02
Start date
2019-07-01
Completion date
2020-06-30
Last updated
2022-08-02

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

Conditions

Acne, Adult

Keywords

acne, observational study, dermocosmetic

Brief summary

The objective of this 3-month observational study was to assess, in 2827 adults, the benefit of NP alone or as adjunctive or maintenance care in mild acne, or as adjunctive care in subjects with moderate acne.

Detailed description

Acne is a chronic inflammatory condition, impacted by exposome factors. A dermocosmetic, Normaderm Phytosolution (NP), was developed to target hyperkeratosis, inflammation, and sebum, while protecting the skin barrier, and to be used either alone or in addition to acne medications. NP is a dermocosmetic specifically developed for acne-prone skin. The lightweight cream is easily absorbed and targets acne pathogenesis thanks to salicylic acid 2% for skin exfoliation, phyco-saccharide 2% for sebum reduction, and vitamin CG as anti-inflammatory ingredient, as well as ingredients that enable regeneration of the disrupted skin barrier, such as Vichy mineralizing water 60%, Bifida ferment lysate 1%, and hyaluronic acid 0.2%. The study was conducted in accordance with the protocol and the legislative and regulatory provisions in force (after obtaining authorization of the French health authorities and the favorable opinion of the ethics committee). Qualitative variables were described as numbers and percentages. 95% confidence intervals (CI) were calculated, where required. Quantitative variables were described as number, mean, standard deviation, median, minimum, maximum and number of missing data. All statistical analyses were performed at a 5% significance using 2-sided tests, except normality, tested at the threshold of 1% (Shapiro-Wilk test).

Interventions

DRUGNormaderm Phytosolution Double-Correction Daily Care Moisturizer

Normaderm Phytosolution (NP) was to be applied for up to 90 days once or twice daily, according to the investigator's prescription.

Sponsors

Cosmetique Active International
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adult men or women (age \>18 years old) with mild to moderate acne (GEA scale 1-3).

Exclusion criteria

Patients taking isotretinoin. Patients presenting with highly inflammatory acne, grade 4 or 5 on the GEA scale. Patients presenting with nodules.

Design outcomes

Primary

MeasureTime frameDescription
Benefit of NP alone or as adjunctive or maintenance care in mild acne, or as adjunctive care in subjects with moderate acne.90-day useChange in global acne severity using a scale from 0=none to 5 very severe (GEA scale)

Secondary

MeasureTime frameDescription
Change in seborrhea level90-day useassessed on a visual analog scale from 0 (absent) to 10 (severe
Change in skin hydration90-day useassessed on a visual analog scale from 0=no hydration to 10=perfectly hydrated

Countries

Argentina, Bulgaria, Czechia, Germany, Hungary, Mexico, Poland, Romania, Russia, Slovakia, Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026