Safety and Efficacy assessment of Product on ski
- Registration Number
- CTRI/2022/06/043478
- Lead Sponsor
- Sun Pharmaceutical Industries Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Indian male & female subjects
2.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)
3.Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar�.)
4.Being able to produce at least 100 mg of sweat and whose left versus right half face sweat is more or less the same
5.Having shaved beard two days before study visit.
1.For Females: Being pregnant or breastfeeding or having stopped to breastfeed in the past three months.
2.Having refused to give his/her assent by not 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.Having sensitive or dry skin & acne prone skin.
6.Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months)
7.Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products or food products.
8.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).
9.Having cutaneous hypersensitivity.
10.Having undergone a surgery requiring a general anaesthetic of more than one hour in the past 6 months.
11.Having changed 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.Refusing to follow the restrictions below during the study:For Females: Do not take part in any family planning activities leading to pregnancy and breastfeeding; Do not take part in another study liable to interfere with this study.; Do not take 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); Do not change their cosmetic habits apart from the particular conditions mentioned in the protocol, on the studied anatomic unit; Do not have sensitive or dry skin & acne prone skin.; During the study: Do not use other cosmetic products than the tested products to the studied areas.; The day of the measurements: No test product must be used (only face cleaned with water is accepted); The day of the measurements: Do not apply hair oil.
14.Having started, changed or interrupted one hormonal treatment (hormonal contraception, Hormone Replacement Therapy) during the past 3 months
15.Having started, changed or stopped his/her tobacco consumption (for smokers consuming more than 10 cigarettes per day) in the previous 6 months
16.Not having shaved beard two days before study visit.
17.Having applied oil one day prior study visit.
18.Refusing to follow the restrictions below during the study:Do not start, change or stop a hormonal treatment (hormonal contraception, Hormone Replacement Therapy); Do not have beauty treatment (e.g. skin cleansing, exfoliation, scrub, mask �) ; Do not practice water activities (swimming pool, sauna, hammam); Do not practice sport the day of the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method sweat resistance, safetyTimepoint: Day 1: 30 minutes after product application, Day 2: 30 minutes after product application
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI