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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03276897
Other study ID # E0517
Secondary ID
Status Completed
Phase N/A
First received September 4, 2017
Last updated September 6, 2017
Start date March 21, 2017
Est. completion date June 30, 2017

Study information

Verified date September 2017
Source Derming SRL
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Efficacy and Tolerance Evaluation of a"revitalizing" face treatment consisting of a day and a night cream


Description:

Aim of the study was to evaluate clinically and by non-invasive instrumental evaluations the activity of a "revitalizing" face treatment consisting of a day and a night cream, applied for an uninterrupted period of 3 months, by female volunteers, aged 35-60 years, with aging/photo aging of moderate grade.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date June 30, 2017
Est. primary completion date June 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 35 Years to 60 Years
Eligibility Inclusion Criteria:

- female sex,

- age 35-60 years,

- Caucasian subjects,

- presence of moderate face ritidosis,

- agreeing to present at each study visit without make-up,

- accepting to follow the instructions received by the investigator,

- accepting to not change their habits regarding food, physical activity, face cleansing and make- up use,

- agreeing not to apply or take any product or use face massages or other means known to improve skin wrinkle and skin qualities during the entire duration of the study,

- accepting not to expose their face to strong UV irradiation (UV session, or sun bathes), during the entire duration of the study,

- no participation in a similar study currently or during the previous 3 months

- accepting to sign the Informed consent form.

Exclusion Criteria:

- Pregnancy,

- lactation,

- sensitivity to the test products or their ingredients (to be assessed by the investigator during the baseline visit),

- subjects whose insufficient adhesion to the study protocol is foreseeable.

- presence of cutaneous disease on the tested area as lesions, scars, malformations,

- recurrent facial/labial herpes,

- clinical and significant skin condition on the test area (e.g. active eczema, dermatitis, psoriasis etc.).

- endocrine disease,

- hepatic disorder,

- renal disorder,

- cardiac disorder,

- pulmonary disease,

- cancer,

- neurological or psychological disease,

- inflammatory/immunosuppressive disease,

- drug allergy.

- anti-inflammatory drugs, anti-histaminic, topic (application on the face) and systemic corticosteroids, narcotic, antidepressant, immunosuppressive drugs (with the except of hormonal treatment starting more than 1 year ago),

- using of drugs or dietary supplements able to influence the test results in the investigator opinion.

Study Design


Related Conditions & MeSH terms

  • Face Aging/Photo Aging of Moderate Grade

Intervention

Other:
Nutriage SPF 30 day cream and Nutriage night cream (Difa Cooper S.p.a, Italy)
A fixed quantity of both cosmetic products was applied for an uninterrupted period of 3 months, on the face included the submental area (day cream at the morning and the night cream at the evening), preferentially always at the same hour, with a mild massage

Locations

Country Name City State
Italy DERMING Monza Monza-brianza

Sponsors (1)

Lead Sponsor Collaborator
Derming SRL

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of wrinkles grade, around the eyes (Crow's feet) Variation of wrinkles grade from baseline of the Glogau's reference photographic scale (visual score from 1-4) where:
Type 1: early wrinkles
Type 2: wrinkle in motion
Type 3: wrinkles at rest
Type 4: Only wrinkles
Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)
Primary Change of wrinkles grade of nasolabial folds Variation of wrinkles grade from baseline of the Lemperle's reference photographic scale (visual score from 1-6) where:
Grade 1: no wrinkles
Grade 2: just perceptible wrinkles
Grade 3: shallow wrinkles
Grade 4: moderately deep wrinkles
Grade 5: deep wrinkles, well-defined folds
Grade 6: very deep wrinkles, redundant fold
Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)
Primary Change of skin surface microrelief's regularity Variation of skin surface microrelief's regularity grade from baseline of cheek surface microrelief photographic scale where:
Grade 1:very regular
Grade 2: regular
Grade 3: irregular
Grade 4: very irregular.
Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)
Primary Change of skin resistance to pinching clinical score The evaluation was performed at level of cheek (malar region) according to the following score:
0 = very important
= important
= moderate
= weak
= very weak
Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)
Primary Change of skin resistance to traction clinical score The evaluation was performed at level of cheek (malar region) according to the following score:
0 = very important
= important
= moderate
= weak
= very weak
Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)
Primary Change of skin recovery after pinching clinical score The evaluation was performed at level of cheek (malar region) according to the following score:
0 = very important
= important
= moderate
= weak
= very weak
Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)
Primary Change of skin dryness clinical score Clinical evaluation of skin dryness was performed according to the following score:
0 = very hydrated skin
= hydrated skin
= normal skin
= kindly dry skin
= dry skin
= very dry skin
Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)
Primary Change of vascular and pigmentary homogeneity clinical score Homogeneity grade was determined according to specific reference clinical and photographic scales and to the following clinical score:
0 = very homogeneous
= homogeneous
= quite not homogeneous
= not homogeneous
= very not homogeneous
= marked not homogeneous
Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)
Secondary Change of roughness profilometric parameters Crow's feet profilometric parameters measured by Primos compact portable device (GFMesstechnik). Ra is average roughness of the analysed profile, Rt is wrinkles total high, Rv is wrinkles maximum depth. Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)
Secondary Photographic documentation (3D pictures) Three-dimensional pictures of the face taken by VECTRA H1 handheld imaging system. Baseline visit (T0), 1 month (T1), 2 months (T2), 3 months (T3)