A clinical study to evaluate the safety and efficacy of Nimson Kesh silk Plus oil in controlling hairfall and premature greying

Not Applicable

Completed

• Conditions: Medical and Surgical. Ayurveda Condition: KHALITYAM/KHALATI,

• Registration Number: CTRI/2023/06/054313
• Lead Sponsor: Aryanveda Cosmeceuticals

Brief Summary

This study is an prospective , single arm,open label, single centre clinical study to evaluate the safety and efficacy of Nimson Keshsilk Plus oil in Controlling Hair fall and premature greying

Primary Objective :

• Prevention or control of premature greying of hair

• Reduced hair fall ensuring thicker and stronger hair growth.



Secondary Objective :

• To test the ability of the test product to nourish the hair measured by measuring the length and strand

Detailed Description

Not available

Study Timeline

• Study Start: 2023-03-07
• Study Completion: 2023-08-15
• Last Update Posted: 2024-03-19

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Subjects aged between 18 to 65 years.
• Patients having Khalitya (Baldness) and Palitya (premature Greying) as per Ayurvedic classical texts and as per modern parameters i.e., Hair fall, Dandruff and Dryness of hairs have been selected irrespective of any bar of caste, gender, religion and occupation.

Exclusion Criteria

• Signs of allergy, irritation or intolerance to the components of the test product Patients who have been diagnosed to have local disease like Alopecia areata, Alopecia totalis, Tinea capitis, Folliculitis devaculans.
• Patient with hair fall related to any Systemic disorders, any Hormonal disorders, Post CA treatments and Vitiligo.
• Pregnancy or lactation.
• Participation in other clinical trials.
• Unwilling/unable to sign the informed consent.

Study & Design

• Study Type: PMS
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
• Reduced hairfall as per the 60 seconds hairfall on Day 28 when compared with the baseline value	day 28
• Improvement in the Greying Severity score in comparison with the baseline	day 28

Secondary Outcome Measures

Name	Time	Method
• Increase in hair length to establish the ability of the oil to Nourish the hair.	• Number of subjects experiencing eye or skin irritation or any adverse events in the treatment phase.

Trial Locations

Locations (1)

Dr. Uday’s Advance Skin and Hair clinic; 🇮🇳 Bangalore, KARNATAKA, India

Dr. Uday’s Advance Skin and Hair clinic

🇮🇳Bangalore, KARNATAKA, India

Dr Uday Kumar

Principal investigator

6364147980

info@samahitha.com