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CTRI Number  CTRI/2022/03/041070 [Registered on: 14/03/2022] Trial Registered Prospectively
Last Modified On: 01/04/2022
Post Graduate Thesis  No 
Type of Trial  PMS 
Type of Study   Ayurveda
Other (Specify) [cosmetic product category]  
Study Design  Single Arm Study 
Public Title of Study   A clinical study to check intensive hair repair masque in healthy volunteers for its safety and efficacy. 
Scientific Title of Study   A SINGLE CENTRE PROSPECTIVE DERMATOLOGICAL STUDY TO EVALUATE PARAMETERS ON HAIR THAT DEEPLY NOURISHES HAIR, REPAIR DRY & DAMAGE HAIR, STRENGHTEN, PROTECT HAIR FROM HEAT & DAMAGE & BRINGS GLOSS, SHINE WITH (INTENSIVE HAIR REPAIR MASQUE) IN HEALTHY VOLUNTEERS. 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
MVS/CPS/07/2022,Version: 1.0 Dated: 10 January 2022  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Esha Roy 
Designation  Principal Investigator (Dermatologist) 
Affiliation  Qaaf Healthcare International  
Address  Clinical Division, A-62, Basement Room No. B01, DDA Shed
Okhla Industrial Area, Phase II
South
DELHI
110020
India 
Phone  9254425442  
Fax    
Email  esharoy86@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Mr Nishant Singh 
Designation  Deputy Manager Regulatory Affairs  
Affiliation  Mountain Valley Springs India Pvt. Ltd. 
Address  B12, Block B, Sector 3, Noida

Gautam Buddha Nagar
UTTAR PRADESH
201301
India 
Phone  08860800289  
Fax    
Email  nishant.singh@forestessentialsindia.com  
 
Details of Contact Person
Public Query
 
Name  Mr Nishant Singh 
Designation  Deputy Manager, Regulatory Affairs  
Affiliation  Mountain Valley Springs India Pvt. Ltd. 
Address  B12, Block B, Sector 3, Noida

Gautam Buddha Nagar
UTTAR PRADESH
201301
India 
Phone  08860800289  
Fax    
Email  nishant.singh@forestessentialsindia.com  
 
Source of Monetary or Material Support  
Mountain Valley Springs India Pvt. Ltd. India 
 
Primary Sponsor  
Name  Mountain Valley Springs India Pvt Ltd  
Address  Mountain Valley Springs India Pvt. Ltd. India B12 Block B Sector 3 Noida Uttar Pradesh India 
Type of Sponsor  Other [Cosmetic Company] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Esha Roy  Qaaf Healthcare International   Clinical Division, A-62, Basement Room No. B01, DDA Shed, Okhla Industrial Area, Phase II, New Delhi-110020
South
DELHI 
9254425442

esharoy86@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Society for research welfare Independent ethics committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  The objective of this study is to evaluate the efficacy of Intensive hair Repair Masque on healthy human subjects. 
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmDrugOther than Classical(1) Medicine Name: Japapatti and Brahmi , Reference: NA, Route: Topical, Dosage Form: , Dose: 10(ml), Frequency: bd, Bhaishajya Kal: , Duration: , anupAna/sahapAna: No, Additional Information:
(2) Medicine Name: 30 Days, Reference: NA, Route: NA, Dosage Form: , Dose: (), Frequency: , Bhaishajya Kal: , Duration: , anupAna/sahapAna: No, Additional Information:
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  65.00 Year(s)
Gender  Both 
Details  Healthy subjects (no infectious and evaluative pathology which could make the
subject vulnerable and stop the study, no pathology which could interfere with the
study, no symptom in the process of an exploratory check-up)
Indian Male/Female subjects.
Hair & scalp is healthy on the studied anatomic unit (free of eczema, wounds,
inflammatory scar etc)
Between 18 to 65 years of age, with normal Hair condition.
Written informed consent signed by the subject in line with applicable regulation
of country. 
 
ExclusionCriteria 
Details  Having refused to give her consent by not signing the consent form.
Taking part in another study liable to interfere with this study.
Having a chronic dermatosis liable to modify the cutaneous reactivity on the
tested area (except for specific studies on a determined dermatosis).
Having a diagnosed or highly probable allergy to one or several compounds of
the cosmetic products or food products.
Having cutaneous hypersensitivity.
Having applied a cosmetic product (included make-up) on the studied areas the
first day of the study (only hair & scalp cleaned with water is accepted). 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
Evaluation will include assessment of local adverse events of redness, itching, rashes and burning sensations and any other local side effect and will be categorized non serious (based on severity grades, patterns, and causality) and serious adverse events. There will be two types of assessment, subject self-assessment, and dermatological evaluation by study investigator  Subject will be assesed at 30 minutes, 15 days and 30 days of first application 
 
Secondary Outcome  
Outcome  TimePoints 
Nil  Nil 
 
Target Sample Size   Total Sample Size="50"
Sample Size from India="50" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Post Marketing Surveillance 
Date of First Enrollment (India)   21/03/2022 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="0"
Months="2"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Closed to Recruitment of Participants 
Publication Details   NIL 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary   It is a single centre, prospective, open label, non-comparative dermatological study to evaluate the parameters on hair that deeply nourishes hair, repair dry and damaged hair, strengthen and protect hair from heat brings gloss and shine using Intense Hair Repair Masque in healthy volunteers. This study will be conducted in compliance with applicable national regulations for Post Marketing Surveillance of cosmetic product with the aim of identifying or quantifying safety hazards relating to an authorized cosmetic product and is aligned with various guidelines and recommendations for guideline on PMS practices for cosmetic products.  

 
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