None listed
Conditions
Interventions
Intervention1: Roll On - Product A: Product is applied on one randomized underarm. once in a day for period of 3 days.
Intervention2: Product B: Product is applied on one randomized underarm. once in
Sponsors
ITC LIMITED
Eligibility
Inclusion criteria
Inclusion criteria: 1)Healthy subjects 2)Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar….) 3)Having mild to moderate malodour. 4)Having sweat and visible underarm pigmentation 5)Having shaved under arms two days before each study visit. 6)Having mild to moderate axillary odour and whose left vs right axillary odour levels are more or less the same. 7)Subjects representing varied skin 8)Exhibiting good tolerance to the investigational product with no signs of sensitivity.
Exclusion criteria
Exclusion criteria: 1)For Females: Being pregnant or breastfeeding or having stopped to breastfeed in the past three months. 2) Having refused to give 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 a progressive asthma. 6) Being epileptic. 7) Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months) 8) Having cutaneous hypersensitivity 9) Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products. 11) 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) and/or smoked in the two hours preceding the measurements 12) Having undergone a surgery requiring a general anaesthetic of more than one hour in the past 6 months. 13) Having changed her cosmetic habits in the 14 days preceding the start of the study on the studied anatomic unit 14) Having applied a cosmetic product (included make-up) or skin care product on the studied areas the day of the study (only face cleaned with water is accepted)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Controlling Sweat and Sweat malodorTimepoint: Baseline, Immediate after application, 8Hours, 24 hours, Day 3, Day 6 | — |
Secondary
| Measure | Time frame |
|---|---|
| Reducing Axillary hyperpigmentation and enhancing skin MoisturizationTimepoint: Baseline, Immediate after application, 8Hours, 24 hours, Day 3, Day 6 | — |
Countries
India
Contacts
Public ContactDr Mohit Lalvani
MASCOT-SPINCONTROL India Pvt. Ltd.
Outcome results
None listed