MedPath

Safety and efficacy of skin care formulatio

Not Applicable
Registration Number
CTRI/2021/08/035607
Lead Sponsor
Kama Ayurveda Pvt Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Having dull skin and uneven skin tone

Having pigmentary spot on the face

Having Crows feet wrinkle of grade 2

Having visible under eye dark circle

Exclusion Criteria

Having started, changed or interrupted one hormonal treatment (hormonal contraception,

Hormone Replacement Therapy) during the past 3 months

Having started, changed or stopped her tobacco consumption (for smokers consuming more

than 10 cigarettes per day) in the previous 6 months

Having consumed caffeine-based products (coffee, cola, tea, â?¦), alcohol, highly spiced food

and/or not smoke in the two hours preceding the measurements

Having taken a medicinal treatment which could lead to hyper pigmentation (phenytoïn,

amiodarone, metals, minocyclineâ?¦) in the previous 6 months

• Taking oral supplements with major or minor effect on whitening of skin (e.g. vitamin C,

beta-caroteneâ?¦)

Having had beauty treatment (e.g. skin cleansing, exfoliation, scrub, mask â?¦) or having

applied self-tanning products in the week preceding the start of the study

Having applied products with anti-wrinkle action (Retinoic acid, retinol, retinaldehyde,

isotretinoin, A.H.A...) in the 2 weeks preceding the start of the study

Having applied products with a depigmenting/ whitening action (hydroquinone or

derivatesâ?¦) in the 4 weeks preceding the start of the study.

Having undergone physical and/or chemical treatments of the spots (liquid nitrogen, dry ice,

pulsed flash lamp, dermabrasion, chemical peel â?¦) in the previous 6 months

Having a suntanned skin on the studied areas which could interfere with the evaluations of

the study

For males, having not shaved their beard 24 hours prior to the day of measurement

Study & Design

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