Safety and efficacy of skin care formulatio

Not Applicable

• Registration Number: CTRI/2022/01/039134
• Lead Sponsor: Kama Ayurveda Pvt Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 February 2022

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Having moderate to severe hair fall.

Having Moderate to severe dandruff where 0 is None, 1 is Slight, 2 is Mild, 3 is Moderate, 4

is Severe

Suffering with hair thinning on subject assessment basis.

For female: Having at least shoulder length hair.

Having washed their hair with provided neutral shampoo, 48 hours before the first day of the

study with the provided nuetral shampoo.

Having untangled their hair at home, 3 hours prior coming to the site for observations, the first

day of the study.

Exclusion Criteria

Small, red bumps on the scalp, neck, and shoulders (bumps may become crusty and ooze)

Subject having applied a product with an anti-hair fall claim (due to breakage)or anti dandruff claim in the 2 weeks preceding the start of the study

Having surgery history on the scalp (micro transplants â?¦)

In the previous 6 months

- Having undergone the Minoxidil treatments

- Antiandrogen medicine (cyproterone acetate, spironolactone, flutamide)

- Having undergone one of the following treatments known to : induce hair loss : retinoids, anti coagulants, anti-convulsive drugs, chemotherapy, beta-blocking agents, non steroidal anti inflammatory drugs, corticoids â?¦

- Having modified her hormonal contraception

In the previous 3 months

- Having undergone a local or general anti hair loss treatment (Biotine, dexpanthenol, sulphur amino-acid, B6 vitamin, zinc â?¦)

- Having taken a food supplement with an anti hair loss claim

- Having taken an iron based treatment

In the previous 15 days

- Having applied a product with an anti hair loss claim (due to breakage) or anti dandruff claim

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
efficacy of hair care formulation in <br/ ><br>terms of reduction in Hair Fall and Anti-dandruff effectTimepoint: T0, T14 days and T28 days

Secondary Outcome Measures

Name	Time	Method
SafetyTimepoint: T0, T14 days and T28 days