CTRI/2023/11/059467
Not yet recruiting
未知
To evaluate the in-vivo safety and efficacy of Hair care formulation in terms of reduction in hair fall and improvement in hair growth (Hair Length) on healthy female subjects. - NI
Vansaar0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Vansaar
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\)Indian female subjects.
- •2\)Healthy subjects
- •3\)Skin \& scalp is healthy on the studied anatomic unit
- •4\) Having moderate to severe hair fall
Exclusion Criteria
- •1\)Being insulin\-dependent diabetic or non insulin\-dependent diabetic with a recent therapy (less than 6 months)
- •2\) Having a progressive asthma (either under treatment or last fit in the last 2 years)
- •3\) Being epileptic
- •4\) Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months)
- •5\) Having cutaneous hypersensitivity
- •6\) Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products
- •7\) Following a chronic or intermittent medicinal treatment comprising any of the following products: aspirin\-based products, anti\-inflammatories, anti\-histamines, anti\-coagulants, corticotherapy, taken by general or local routes (the only medication permitted is paracetamol)
- •8\) Having undergone a surgery requiring a general anaesthetic of more than one hour in the past 6 months
- •9\) Having changed his/her cosmetic habits except those required by the protocol in the 14 days preceding the start of the study on the studied anatomic unit.
- •10\) Having applied a hair care product and cosmetic product on the studied area as well as on the face the first day of the study (except the neutral shampoo without anti hairfall claim or hair growth claim)
Outcomes
Primary Outcomes
Not specified
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