MedPath

Efficacy check of cosmetic product

Not Applicable
Registration Number
CTRI/2024/06/068848
Lead Sponsor
AVT Natural Products Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1)Healthy subjects (no infectious and evolutive pathology which could make the subject vulnerable and stop the study, no pathology which could interfere with the study, no symptom in the process of an exploratory checkup)

2)Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar….)

3)Having mild to moderate acne 4)Facial skin and sebum level of forehead more than 100 µg/cm2 5)Having acne PIH dark spots

Exclusion Criteria

1)Being pregnant or breastfeeding or having stopped to breastfeed in the past three months.

2)Having refused to give her/his assent by signing the consent form.

3)Taking part in another study liable to interfere with this study.

4)Being insulin-dependent diabetic or non insulin-dependent diabetic with a recent therapy (less than 6 months).

5)Being asthmatic.

6)Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products or food products or to latex.

7)Following a chronic medicinal treatment comprising any of the following products: aspirin-based products, anti-inflammatories, anti-histamines, corticotherapy, taken by general or local routes (the only medication permitted is paracetamol).

8)Having cutaneous hypersensitivity.

9)Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products.10)Having undergone a surgery requiring a general anaesthetic of more than one hour in the past 6 months.

11)Having changed his/her cosmetic habits in the 14 days preceding the start of the study on the studied anatomic unit.

12)Having applied a cosmetic product (included make-up) on the studied areas the first day of the study (only face cleaned with water is accepted).

13)Subjects receiving steroids or antihistamine medications or receiving isotretinoin for treating other conditions.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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