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Influence of of Cream With the Silver Fir Wood Extract (Belinal) on Skin

Placebo Controlled Study of Influence of Cream With the Silver Fir (Abies Alba) Wood Extract on the Skin

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02603029
Enrollment
10
Registered
2015-11-11
Start date
2015-03-31
Completion date
2015-07-31
Last updated
2016-03-08

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

Conditions

Ageing, Photoprotection, Skin Care, Skin Cream, Wrinkles

Keywords

skin rejuvenation, anti-ageing effects, minimal erythema dose, dermis structure, physiological skin condition, wrinkling

Brief summary

Objective of the study is to determine the influence of the cream with Silver fir wood (Abies alba) extract (Belinal) on the skin parameters and functions in comparison to the placebo cream. 10 healthy female subjects will use the test cream on one half and placebo cream on the other half of the face and of the gluteal part twice a day for 12 weeks. Various face skin parameters will be evaluated before the cream use (the baseline), after 6 and after 12 weeks of the cream use. To evaluate the photoprotective potential of Belinal the minimal erythema dose (MED) will be determined before (the baseline) and after 12 weeks of the cream use at the gluteal area.

Detailed description

Objective of the study is to determine the influence of the cream with Silver fir wood (Abies alba) extract (Belinal; 2% cream) on the skin parameters and functions in comparison to the placebo cream. 10 healthy female subjects will use the test cream on one half and placebo cream on the other half of the face and of the gluteal area (split-face and split-gluteal area ) twice a day for 12 weeks. Face skin parameters will be evaluated before the cream use (the baseline), after 6 and after 12 weeks of the cream use. The photoprotective potential of Belinal will be evaluated with a determination of the minimal erythema dose (MED) at the gluteal area before (the baseline) and after 12 weeks of the cream use. Comparison will be done as the mean of the individual ratios. The differences between the before-after condition will be analyzed with the statistical test of analysis of variance. In case of failure to find homogeneity in the variances the nonparametric ANOVA, the Willcoxon test, will be used. The results will be expressed as mean ± standard error for each group with a significance level of 0.05 for all the statistical tests.

Interventions

OTHERPlacebo cream

Subjects will use placebo cream twice per day for 12 weeks on one half of the face and of the gluteal area.

OTHERBelinal cream

Subjects will use Belinal cream twice per day for 12 weeks on the other half of the face and of the gluteal area.

Sponsors

Abies Labs d.o.o.
CollaboratorINDUSTRY
VIST - Faculty of Applied Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Signs of skin aging (mimic wrinkles/ fine lines/ poor skin tone/ photoaged skin), * Phototype II and III.

Exclusion criteria

* Allergy to ingredients of tested products * Diagnosed diabetes * Thyroid disease * Inflammatory dermatoses * Regular use of dietary supplements 6 months or less before start of the study, * Invasive rejuvenation treatments (botox injections, hyaluronic acid fillers, needle rollers, needle mesotherapy, etc.) 6 months or less prior to start of the study, * Non-invasive rejuvenation treatments (radiofrequency, electrotherapy, ultrasound therapy, no-needle mesotherapy, etc.) 3 months or less prior to start of the study, * Regular, at least 14 day use of anti-aging cosmetic products containing peptides/ polyphenols/ stem cells extracts/ vitamins in high concentration/ AHAs/ BHAs/ vitamin A or its derivatives) three months or less prior to start of the study, * Gluteal hyperpigmentation, * Expected sunbathing (also in solariums) within the study period.

Design outcomes

Primary

MeasureTime frameDescription
Improvement of photoprotective function of the skinup to 12 weeks of the supplementationMinimal erythema dose (MED) of the skin will be determined. Skin on the gluteal part of the body will be exposed to 10 different doses of UVB light and 24 hours after exposure MED will be determined. Higher MED indicates better photoprotective function of the skin.
Improvement of the dermis structureup to 12 weeks of Belinal cream useUltrasound (US) images of the dermis will be taken and intensity of the dermis determined. Higher intensity of the dermis US images indicates improvement of the collagen and elastin network.

Secondary

MeasureTime frameDescription
Reduction of trans-epidermal water loss6 and 12 weeks of Belinal cream useTrans-epidermal water loss (TEWL) will be measured on the face using open-chamber probe. Lower TEWL indicates better skin barrier function and improved skin condition.
Improved skin hydration6 and 12 weeks of Belinal cream useSkin hydration will be measured on the face.
Reduction of the volume of the periorbital facial wrinkles6 and 12 weeks of Belinal cream useVolume of selected periorbital wrinkles will be quantitatively assessed using CSI programme.
An increase of the dermis thickness6 and 12 weeks of Belinal cream useDermis thickness will be measured with ultrasound imaging of the skin.
Improved skin elasticity6 and 12 weeks of Belinal cream useSkin elasticity will be measured on the face.
Reduction of the area of the periorbital facial wrinkles6 and 12 weeks of Belinal cream useArea of selected periorbital wrinkles will be quantitatively assessed using CSI programme.

Outcome results

None listed

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